nicotinic acid ๐Ÿถ Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | BioActivity |

Stem definitionDrug idCAS RN
nicotinic acid or nicotinoyl alcohol derivatives 2835 59-67-6

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • niacin potassium
  • niacin magnesium
  • nicotinic acid
  • vitamin b3 (niacin)
  • 3-pyridinecarboxylic acid
  • niaspan
  • niacin
  • niacor
  • Vitamin B3
A water-soluble vitamin of the B complex occurring in various animal and plant tissues. It is required by the body for the formation of coenzymes NAD and NADP. It has PELLAGRA-curative, vasodilating, and antilipemic properties.
  • Molecular weight: 123.11
  • Formula: C6H5NO2
  • CLOGP: 0.80
  • LIPINSKI: 0
  • HAC: 3
  • HDO: 1
  • TPSA: 50.19
  • ALOGS: -0.17
  • ROTB: 1

  • Status: OFP

  • Legend:
    OFP - off patent
    OFM - off market
    ONP - on patent

Drug dosage:

DoseUnitRoute
0.20 g O
0.20 g P
2 g O

ADMET properties:

PropertyValueReference
BDDCS (Biopharmaceutical Drug Disposition Classification System) 1 Benet LZ, Broccatelli F, Oprea TI
S (Water solubility) 16.66 mg/mL Benet LZ, Broccatelli F, Oprea TI
MRTD (Maximum Recommended Therapeutic Daily Dose) 101.53 ยตM/kg/day Contrera JF, Matthews EJ, Kruhlak NL, Benz RD

Approvals:

DateAgencyCompanyOrphan
July 24, 1957 FDA MEDPOINTE PHARM HLC

FDA Adverse Event Reporting System (Female)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Flushing 460.48 12.94 263 14304 69837 56207663
Drug hypersensitivity 207.36 12.94 302 14265 274903 56002597
Skin burning sensation 122.65 12.94 59 14508 10972 56266528
Pruritus 115.20 12.94 253 14314 316370 55961130
Paraesthesia 49.19 12.94 106 14461 130408 56147092
Product residue present 47.40 12.94 22 14545 3773 56273727
Myalgia 43.89 12.94 102 14465 131923 56145577
Feeling hot 43.72 12.94 54 14513 41733 56235767
Erythema 42.86 12.94 112 14455 155827 56121673
Urticaria 41.92 12.94 106 14461 144570 56132930
Rheumatoid arthritis 41.19 12.94 24 14543 382580 55894920
Infusion related reaction 37.25 12.94 5 14562 208926 56068574
Rhabdomyolysis 36.96 12.94 49 14518 40609 56236891
Burning sensation 31.56 12.94 50 14517 48646 56228854
Blood triglycerides increased 30.87 12.94 25 14542 11652 56265848
Discoloured vomit 29.32 12.94 10 14557 763 56276737
Systemic lupus erythematosus 28.36 12.94 6 14561 180072 56097428
Coronary artery disease 27.81 12.94 37 14530 30759 56246741
Femoral artery dissection 26.58 12.94 5 14562 30 56277470
Glossodynia 26.34 12.94 4 14563 152454 56125046
Low density lipoprotein increased 25.57 12.94 17 14550 5857 56271643
Sinoatrial block 24.67 12.94 9 14558 837 56276663
Off label use 24.39 12.94 69 14498 556111 55721389
Drug ineffective 22.91 12.94 142 14425 918847 55358653
Blood glucose increased 20.64 12.94 54 14513 75097 56202403
Maternal exposure during pregnancy 20.20 12.94 12 14555 189541 56087959
Completed suicide 19.99 12.94 5 14562 133828 56143672
Lower respiratory tract infection 19.85 12.94 3 14564 114791 56162709
Myopathy 19.80 12.94 18 14549 9794 56267706
Treatment failure 19.30 12.94 10 14557 170382 56107118
Wound 19.21 12.94 6 14561 138798 56138702
Neutropenia 18.33 12.94 9 14558 158158 56119342
Blood cholesterol abnormal 18.03 12.94 10 14557 2490 56275010
General physical health deterioration 17.78 12.94 11 14556 169999 56107501
Cyst 17.54 12.94 19 14548 12759 56264741
Pyrexia 16.86 12.94 54 14513 418719 55858781
Stress 15.83 12.94 42 14525 58868 56218632
Febrile neutropenia 15.65 12.94 4 14563 105541 56171959
High density lipoprotein decreased 15.38 12.94 8 14559 1754 56275746
Hyperlipidaemia 15.19 12.94 21 14546 18088 56259412
Swelling face 15.10 12.94 40 14527 56029 56221471
Condition aggravated 14.92 12.94 43 14524 344855 55932645
Internal haemorrhage 14.31 12.94 11 14556 4753 56272747
Blood magnesium increased 13.97 12.94 9 14558 2942 56274558
Bicytopenia 13.94 12.94 8 14559 2125 56275375
Low turnover osteopathy 13.70 12.94 10 14557 3998 56273502
Chest pain 13.68 12.94 90 14477 189707 56087793
Product use in unapproved indication 13.53 12.94 10 14557 140812 56136688
Angina pectoris 13.23 12.94 25 14542 27951 56249549
Pain in extremity 13.16 12.94 126 14441 297305 55980195

FDA Adverse Event Reporting System (Male)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Flushing 920.30 12.96 422 19047 29706 31648169
Product residue present 230.07 12.96 79 19390 2551 31675324
Pruritus 115.40 12.96 244 19225 124923 31552952
High density lipoprotein decreased 108.13 12.96 48 19421 3102 31674773
Myalgia 93.49 12.96 169 19300 77089 31600786
Myocardial infarction 75.75 12.96 195 19274 113259 31564616
Skin burning sensation 74.67 12.96 40 19429 3899 31673976
Off label use 58.33 12.96 77 19392 347197 31330678
Drug hypersensitivity 57.14 12.96 133 19336 72466 31605409
Blood glucose increased 48.15 12.96 112 19357 60971 31616904
Feeling hot 47.25 12.96 54 19415 16179 31661696
Blood creatine phosphokinase increased 45.92 12.96 88 19381 41886 31635989
Toxicity to various agents 44.97 12.96 28 19441 181459 31496416
Coronary artery disease 44.85 12.96 92 19377 45995 31631880
Burning sensation 40.98 12.96 51 19418 16696 31661179
Blood triglycerides increased 39.72 12.96 45 19424 13352 31664523
Coronary artery occlusion 38.11 12.96 39 19430 10317 31667558
Paraesthesia 37.98 12.96 97 19372 55974 31621901
Respiratory tract infection bacterial 36.82 12.96 18 19451 1448 31676427
Low density lipoprotein increased 32.70 12.96 24 19445 4064 31673811
Respiratory tract infection viral 31.44 12.96 18 19451 1996 31675879
Rhabdomyolysis 31.31 12.96 98 19371 63483 31614392
Product use in unapproved indication 31.15 12.96 11 19458 99160 31578715
Febrile neutropenia 24.77 12.96 23 19446 121826 31556049
Completed suicide 24.22 12.96 13 19456 91501 31586374
Blood cholesterol increased 23.04 12.96 39 19430 16854 31661021
Dyspepsia 22.74 12.96 57 19412 32496 31645379
Injury 22.38 12.96 42 19427 19667 31658208
Product use issue 22.23 12.96 4 19465 56755 31621120
Erythema 21.44 12.96 102 19367 80303 31597572
Death 21.37 12.96 132 19337 360437 31317438
Dizziness 21.31 12.96 201 19268 198946 31478929
General physical health deterioration 21.24 12.96 23 19446 113412 31564463
Muscle spasms 20.70 12.96 90 19379 68228 31609647
Neutropenia 20.65 12.96 34 19435 140330 31537545
Myopathy 20.32 12.96 29 19440 10823 31667052
Hot flush 20.27 12.96 36 19433 16160 31661715
Transaminases abnormal 19.57 12.96 7 19462 255 31677620
Chest pain 17.86 12.96 128 19341 116829 31561046
Pain in extremity 16.50 12.96 125 19344 116078 31561797
Cerebrovascular accident 16.46 12.96 94 19375 79390 31598485
Asthenia 15.86 12.96 209 19260 224546 31453329
Foetal exposure during pregnancy 15.75 12.96 3 19466 40873 31637002
Treatment failure 15.70 12.96 3 19466 40789 31637086
Hypoaesthesia 15.61 12.96 72 19397 55950 31621925
Glycosylated haemoglobin increased 15.51 12.96 25 19444 10375 31667500
Gout 15.05 12.96 34 19435 18140 31659735
Angina pectoris 14.86 12.96 46 19423 29595 31648280
Impaired work ability 14.54 12.96 18 19451 5859 31672016
Urticaria 13.92 12.96 71 19398 57446 31620429
Blood testosterone decreased 13.78 12.96 15 19454 4258 31673617
Condition aggravated 13.76 12.96 53 19416 163956 31513919
Renal impairment 13.56 12.96 20 19449 86329 31591546
Cardiac failure 13.41 12.96 20 19449 85933 31591942
Flatulence 13.04 12.96 33 19436 18915 31658960
Gastrointestinal haemorrhage 12.97 12.96 91 19378 82458 31595417

FDA Adverse Event Reporting System (Geriatric)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Flushing 194.02 11.78 182 22943 81990 70823329
Drug hypersensitivity 112.95 11.78 258 22867 262201 70643118
Myocardial infarction 102.31 11.78 193 22932 171452 70733867
Coronary artery disease 89.01 11.78 106 23019 62630 70842689
Myalgia 85.79 11.78 177 22948 167715 70737604
Rhabdomyolysis 71.61 11.78 119 23006 95641 70809678
High density lipoprotein decreased 58.40 11.78 28 23097 4091 70901228
Blood creatine phosphokinase increased 49.68 11.78 79 23046 61184 70844135
Off label use 49.05 11.78 106 23019 742954 70162365
Blood triglycerides increased 45.28 11.78 43 23082 19621 70885698
Respiratory tract infection bacterial 44.83 11.78 18 23107 1719 70903600
Rheumatoid arthritis 32.99 11.78 28 23097 291777 70613542
Respiratory tract infection viral 32.60 11.78 18 23107 3523 70901796
Coronary artery occlusion 32.32 11.78 31 23094 14314 70891005
Completed suicide 32.11 11.78 17 23108 227118 70678201
Contraindicated product administered 30.34 11.78 4 23121 134608 70770711
Myopathy 27.29 11.78 32 23093 18580 70886739
Blood glucose increased 26.66 11.78 84 23041 102898 70802421
Infusion related reaction 26.17 11.78 16 23109 197518 70707801
Angina pectoris 25.83 11.78 52 23073 48331 70856988
Low density lipoprotein increased 25.27 11.78 21 23104 8044 70897275
Product use in unapproved indication 24.57 11.78 19 23106 207459 70697860
Femoral artery dissection 24.28 11.78 5 23120 39 70905280
Febrile neutropenia 23.83 11.78 19 23106 204299 70701020
Cerebrovascular accident 22.06 11.78 99 23026 143371 70761948
Discoloured vomit 22.03 11.78 10 23115 1291 70904028
Cardiac failure congestive 21.99 11.78 95 23030 135362 70769957
General physical health deterioration 21.73 11.78 27 23098 236004 70669315
Treatment failure 21.55 11.78 10 23115 144132 70761187
Acute myocardial infarction 21.25 11.78 62 23063 72825 70832494
Toxicity to various agents 20.85 11.78 60 23065 382112 70523207
Product residue present 20.22 11.78 13 23112 3357 70901962
Chest pain 19.23 11.78 144 22981 251116 70654203
Sinoatrial block 19.15 11.78 9 23116 1257 70904062
Therapy cessation 18.95 11.78 37 23088 33639 70871680
Maternal exposure during pregnancy 18.86 11.78 7 23118 115338 70789981
Glycosylated haemoglobin increased 17.77 11.78 25 23100 17366 70887953
Dizziness 17.75 11.78 230 22895 463911 70441408
Gastrointestinal haemorrhage 17.63 11.78 90 23035 137318 70768001
Condition aggravated 17.40 11.78 76 23049 427559 70477760
Systemic lupus erythematosus 16.97 11.78 6 23119 101896 70803423
Hyperlipidaemia 16.95 11.78 29 23096 23834 70881485
Neutropenia 16.62 11.78 37 23088 257119 70648200
Blood testosterone decreased 16.60 11.78 10 23115 2303 70903016
Angina unstable 16.47 11.78 23 23102 15870 70889449
Lower respiratory tract infection 16.37 11.78 8 23117 111905 70793414
Transaminases abnormal 16.36 11.78 7 23118 785 70904534
Burning sensation 15.44 11.78 45 23080 52825 70852494
Product use issue 15.12 11.78 22 23103 179915 70725404
Drug intolerance 14.97 11.78 32 23093 225655 70679664
International normalised ratio increased 14.97 11.78 59 23066 80667 70824652
Urticaria 14.54 11.78 97 23028 162952 70742367
Blood cholesterol abnormal 14.08 11.78 10 23115 3038 70902281
Muscle spasms 13.95 11.78 92 23033 153954 70751365
Metabolic syndrome 13.51 11.78 9 23116 2466 70902853
Dyspnoea exertional 13.49 11.78 56 23069 78374 70826945
Oedema peripheral 13.31 11.78 123 23002 227968 70677351
Pericardial haemorrhage 13.14 11.78 11 23114 4257 70901062
Pruritus 13.09 11.78 171 22954 345389 70559930
Drug ineffective 13.02 11.78 222 22903 939530 69965789
Coronary artery restenosis 12.99 11.78 7 23118 1305 70904014
Skin burning sensation 12.54 11.78 17 23108 11409 70893910
Pyrexia 12.13 11.78 133 22992 606819 70298500
Paraesthesia 12.03 11.78 85 23040 145452 70759867
Arteriosclerosis coronary artery 11.90 11.78 20 23105 16195 70889124

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
ATC C04AC01 CARDIOVASCULAR SYSTEM
PERIPHERAL VASODILATORS
PERIPHERAL VASODILATORS
Nicotinic acid and derivatives
ATC C10AD02 CARDIOVASCULAR SYSTEM
LIPID MODIFYING AGENTS
LIPID MODIFYING AGENTS, PLAIN
Nicotinic acid and derivatives
ATC C10AD52 CARDIOVASCULAR SYSTEM
LIPID MODIFYING AGENTS
LIPID MODIFYING AGENTS, PLAIN
Nicotinic acid and derivatives
ATC C10BA01 CARDIOVASCULAR SYSTEM
LIPID MODIFYING AGENTS
LIPID MODIFYING AGENTS, COMBINATIONS
Combinations of various lipid modifying agents
FDA CS M0014839 Nicotinic Acids
FDA EPC N0000175594 Nicotinic Acid
MeSH PA D000963 Antimetabolites
MeSH PA D002317 Cardiovascular Agents
MeSH PA D000960 Hypolipidemic Agents
MeSH PA D057847 Lipid Regulating Agents
MeSH PA D018977 Micronutrients
MeSH PA D014665 Vasodilator Agents
MeSH PA D014803 Vitamin B Complex
MeSH PA D014815 Vitamins
CHEBI has role CHEBI:25212 metabolites
CHEBI has role CHEBI:35620 vasodilator agents
CHEBI has role CHEBI:35679 antilipemic drugs
CHEBI has role CHEBI:50247 antidotes
CHEBI has role CHEBI:75771 Mus musculus metabolites
CHEBI has role CHEBI:76924 plant metabolites
CHEBI has role CHEBI:76971 Escherichia coli metabolites
CHEBI has role CHEBI:84087 human urinary metabolites
CHEBI has role CHEBI:84264 nicotinamide deaminase inhibitors
CHEBI has role CHEBI:22586 antioxidants
CHEBI has role CHEBI:23357 cofactor
CHEBI has role CHEBI:61115 histone deacetylase inhibitors
CHEBI has role CHEBI:62913 PARP
CHEBI has role CHEBI:63726 neuroprotective agents
CHEBI has role CHEBI:67079 anti-inflammatory agents
CHEBI has role CHEBI:71181 Sir2 inhibitors
CHEBI has role CHEBI:75772 S. cerevisiae metabolites
CHEBI has role CHEBI:176497 geroprotectors

Drug Use | Suggest Off label Use Form| |View source of the data|

DiseaseRelationSNOMED_IDDOID
Hypercholesterolemia indication 13644009
Hyperlipidemia indication 55822004 DOID:1168
Vitamin deficiency indication 85670002
Familial hypercholesterolemia - heterozygous indication 238079002
Mixed hyperlipidemia indication 267434003
Hypertriglyceridemia indication 302870006




๐Ÿถ Veterinary Drug Use

None

๐Ÿถ Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

Dissociation levelDissociation constantType (acidic/basic)
pKa1 2.31 acidic
pKa2 4.85 Basic

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

TargetClassPharosUniProtActionTypeActivity value
(-log[M])
Mechanism
action
Bioact sourceMoA source
Hydroxycarboxylic acid receptor 2 GPCR AGONIST Ki 7.30 CHEMBL SCIENTIFIC LITERATURE
Nicotinamide N-methyltransferase Enzyme WOMBAT-PK
Nicotinate-nucleotide pyrophosphorylase [carboxylating] Enzyme WOMBAT-PK
Nicotinamide phosphoribosyltransferase Enzyme WOMBAT-PK
Hydroxycarboxylic acid receptor 3 GPCR AGONIST EC50 6.52 IUPHAR
Amyloid beta A4 protein Unclassified IC50 4.88 CHEMBL
Hydroxycarboxylic acid receptor 2 GPCR IC50 6.85 CHEMBL
Hydroxycarboxylic acid receptor 2 GPCR Ki 7.48 CHEMBL

External reference:

IDSource
4019440 VUID
N0000147570 NUI
D00049 KEGG_DRUG
4017632 VANDF
4017661 VANDF
4017718 VANDF
4019440 VANDF
4020285 VANDF
4021898 VANDF
C0027996 UMLSCUI
CHEBI:15940 CHEBI
NIO PDB_CHEM_ID
CHEMBL573 ChEMBL_ID
938 PUBCHEM_CID
DB00627 DRUGBANK_ID
1588 IUPHAR_LIGAND_ID
218728 RXNORM
2275 MMSL
4947 MMSL
5169 MMSL
5170 MMSL
5684 MMSL
7159 MMSL
7161 MMSL
72420 MMSL
d00314 MMSL
d03739 MMSL
001052 NDDF
001055 NDDF
173196005 SNOMEDCT_US
273943001 SNOMEDCT_US
63639004 SNOMEDCT_US
D009525 MESH_DESCRIPTOR_UI
373 INN_ID
2679MF687A UNII

Pharmaceutical products:

ProductCategoryIngredientsNDCFormQuantityRouteMarketingLabel
Niaspan HUMAN PRESCRIPTION DRUG LABEL 1 0074-3074 TABLET, FILM COATED, EXTENDED RELEASE 500 mg ORAL NDA 29 sections
Niaspan HUMAN PRESCRIPTION DRUG LABEL 1 0074-3074 TABLET, FILM COATED, EXTENDED RELEASE 500 mg ORAL NDA 29 sections
Niaspan HUMAN PRESCRIPTION DRUG LABEL 1 0074-3079 TABLET, FILM COATED, EXTENDED RELEASE 750 mg ORAL NDA 29 sections
Niaspan HUMAN PRESCRIPTION DRUG LABEL 1 0074-3079 TABLET, FILM COATED, EXTENDED RELEASE 750 mg ORAL NDA 29 sections
Niaspan HUMAN PRESCRIPTION DRUG LABEL 1 0074-3080 TABLET, FILM COATED, EXTENDED RELEASE 1000 mg ORAL NDA 29 sections
Niaspan HUMAN PRESCRIPTION DRUG LABEL 1 0074-3080 TABLET, FILM COATED, EXTENDED RELEASE 1000 mg ORAL NDA 29 sections
Niaspan HUMAN PRESCRIPTION DRUG LABEL 1 0074-3265 TABLET, FILM COATED, EXTENDED RELEASE 500 mg ORAL NDA 29 sections
Niaspan HUMAN PRESCRIPTION DRUG LABEL 1 0074-3265 TABLET, FILM COATED, EXTENDED RELEASE 500 mg ORAL NDA 29 sections
Niaspan HUMAN PRESCRIPTION DRUG LABEL 1 0074-3274 TABLET, FILM COATED, EXTENDED RELEASE 750 mg ORAL NDA 29 sections
Niaspan HUMAN PRESCRIPTION DRUG LABEL 1 0074-3274 TABLET, FILM COATED, EXTENDED RELEASE 750 mg ORAL NDA 29 sections
Niaspan HUMAN PRESCRIPTION DRUG LABEL 1 0074-3275 TABLET, FILM COATED, EXTENDED RELEASE 1000 mg ORAL NDA 29 sections
Niaspan HUMAN PRESCRIPTION DRUG LABEL 1 0074-3275 TABLET, FILM COATED, EXTENDED RELEASE 1000 mg ORAL NDA 29 sections
VitafolOne HUMAN PRESCRIPTION DRUG LABEL 16 0642-0070 CAPSULE, GELATIN COATED 15 mg ORAL unapproved drug other 14 sections
Vitafol Caplet HUMAN PRESCRIPTION DRUG LABEL 12 0642-0072 CAPSULE 15 mg ORAL UNAPPROVED DRUG OTHER 13 sections
Select OB HUMAN PRESCRIPTION DRUG LABEL 15 0642-0077 TABLET, CHEWABLE 15 mg ORAL UNAPPROVED DRUG OTHER 14 sections
Vitafol OB Caplet HUMAN PRESCRIPTION DRUG LABEL 15 0642-0079 TABLET 18 mg ORAL Unapproved drug other 14 sections
Vitafol Plus HUMAN PRESCRIPTION DRUG LABEL 17 0642-0092 CAPSULE, LIQUID FILLED 15 mg ORAL UNAPPROVED DRUG OTHER 13 sections
Strovite Forte Caplet HUMAN PRESCRIPTION DRUG LABEL 19 0642-0204 TABLET, COATED 100 mg ORAL UNAPPROVED DRUG OTHER 15 sections
Reaphirm Plant Source DHA HUMAN PRESCRIPTION DRUG LABEL 16 0642-3010 CAPSULE, GELATIN COATED 15 mg ORAL unapproved drug other 7 sections
O-Cal Prenatal Vitamin HUMAN PRESCRIPTION DRUG LABEL 16 0813-0202 TABLET 17 mg ORAL UNAPPROVED DRUG OTHER 6 sections
Niacin HUMAN PRESCRIPTION DRUG LABEL 1 10135-612 TABLET, EXTENDED RELEASE 500 mg ORAL ANDA 25 sections
Niacin HUMAN PRESCRIPTION DRUG LABEL 1 10135-613 TABLET, EXTENDED RELEASE 750 mg ORAL ANDA 25 sections
Niacin HUMAN PRESCRIPTION DRUG LABEL 1 10135-614 TABLET, EXTENDED RELEASE 1000 mg ORAL ANDA 25 sections
TriStart DHA HUMAN PRESCRIPTION DRUG LABEL 15 15370-250 CAPSULE, LIQUID FILLED 5 mg ORAL UNAPPROVED DRUG OTHER 12 sections
Niaspan HUMAN PRESCRIPTION DRUG LABEL 1 21695-852 TABLET, FILM COATED, EXTENDED RELEASE 500 mg ORAL NDA 26 sections
Niaspan HUMAN PRESCRIPTION DRUG LABEL 1 21695-865 TABLET, FILM COATED, EXTENDED RELEASE 1000 mg ORAL NDA 26 sections
Niacin Human Prescription Drug Label 1 33342-187 TABLET 500 mg ORAL ANDA 25 sections
Niacin Human Prescription Drug Label 1 33342-189 TABLET 1000 mg ORAL ANDA 25 sections
NIACIN Human Prescription Drug Label 1 47335-539 TABLET, FILM COATED, EXTENDED RELEASE 500 mg ORAL ANDA 27 sections
NIACIN Human Prescription Drug Label 1 47335-539 TABLET, FILM COATED, EXTENDED RELEASE 500 mg ORAL ANDA 27 sections