mupirocin 🐶 Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | BioActivity |

Stem definitionDrug idCAS RN
1857 12650-69-0

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • mupirocin
  • mupricin
  • pseudomonic acid
  • turixin
  • mupirocin calcium
  • bactroban
  • BRL 4910A
A topically used antibiotic from a strain of Pseudomonas fluorescens. It has shown excellent activity against gram-positive staphylococci and streptococci. The antibiotic is used primarily for the treatment of primary and secondary skin disorders, nasal infections, and wound healing.
  • Molecular weight: 500.63
  • Formula: C26H44O9
  • CLOGP: 1.54
  • LIPINSKI: 1
  • HAC: 9
  • HDO: 4
  • TPSA: 146.05
  • ALOGS: -4.28
  • ROTB: 17

  • Status: OFP

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

Drug dosage:

None

ADMET properties:

None

Approvals:

DateAgencyCompanyOrphan
Dec. 31, 1987 FDA GLAXOSMITHKLINE

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
Macular degeneration 741.99 14.84 226 9301 18682 56263858
Chronic sinusitis 95.08 14.84 40 9487 8338 56274202
Drug ineffective 63.48 14.84 314 9213 918675 55363865
Procedural pain 56.79 14.84 35 9492 16236 56266304
Paraesthesia oral 55.37 14.84 33 9494 14416 56268124
Hyperchlorhydria 41.39 14.84 14 9513 1601 56280939
Dyspepsia 39.57 14.84 59 9468 83412 56199128
Therapeutic product effect incomplete 38.02 14.84 66 9461 105965 56176575
Nasal vestibulitis 37.31 14.84 6 9521 20 56282520
Folate deficiency 33.70 14.84 13 9514 2164 56280376
Purpura senile 32.59 14.84 9 9518 520 56282020
Staphylococcal infection 31.06 14.84 35 9492 37583 56244957
Product dose omission issue 30.71 14.84 90 9437 204663 56077877
Tarsal tunnel syndrome 27.89 14.84 8 9519 531 56282009
Toxicity to various agents 27.45 14.84 3 9524 224561 56057979
Weight decreased 27.19 14.84 96 9431 240618 56041922
Hospitalisation 24.70 14.84 45 9482 74955 56207585
Odynophagia 24.64 14.84 15 9512 6803 56275737
Therapy interrupted 23.15 14.84 25 9502 25600 56256940
Resorption bone increased 21.28 14.84 8 9519 1242 56281298
Vestibular disorder 20.82 14.84 8 9519 1317 56281223
Cellulitis 18.66 14.84 40 9487 74909 56207631
Bronchial oedema 17.92 14.84 4 9523 95 56282445
Impetigo 17.72 14.84 7 9520 1241 56281299
Sinusitis 16.74 14.84 72 9455 197509 56085031
Pyrexia 15.83 14.84 123 9404 418650 55863890
Skin infection 15.81 14.84 15 9512 13180 56269360
Vertigo positional 15.56 14.84 8 9519 2621 56279919
General physical health deterioration 15.05 14.84 5 9522 170005 56112535

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
Nasal vestibulitis 52.45 18.06 8 4909 19 31692408
Food aversion 42.20 18.06 10 4907 341 31692086
Dermatitis atopic 36.74 18.06 17 4900 4845 31687582
Staphylococcal infection 31.96 18.06 31 4886 30601 31661826
Toxic epidermal necrolysis 30.85 18.06 25 4892 19499 31672928
Burkholderia test positive 27.52 18.06 9 4908 1013 31691414
Pain of skin 26.80 18.06 13 4904 4113 31688314
Skin discolouration 21.87 18.06 19 4898 16288 31676139
Cheilitis 20.93 18.06 9 4908 2159 31690268
Product dose omission issue 20.09 18.06 48 4869 105538 31586889
Hypophagia 18.77 18.06 20 4897 22022 31670405
Product use in unapproved indication 18.77 18.06 45 4872 99126 31593301
Pruritus 18.75 18.06 52 4865 125115 31567312

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
Macular degeneration 76.43 14.23 33 11702 7495 70909214
Chronic sinusitis 75.94 14.23 34 11701 8417 70908292
Procedural pain 61.77 14.23 38 11697 17971 70898738
Paraesthesia oral 49.01 14.23 31 11704 15386 70901323
Hyperchlorhydria 36.08 14.23 13 11722 1833 70914876
Dyspepsia 34.92 14.23 57 11678 89020 70827689
Food aversion 33.78 14.23 10 11725 759 70915950
Product dose omission issue 33.37 14.23 95 11640 217373 70699336
Weight decreased 31.69 14.23 118 11617 310370 70606339
Toxicity to various agents 31.40 14.23 12 11723 382160 70534549
Therapeutic product effect incomplete 29.72 14.23 63 11672 119819 70796890
Tarsal tunnel syndrome 28.58 14.23 8 11727 497 70916212
Purpura senile 28.49 14.23 8 11727 503 70916206
Cellulitis 28.09 14.23 55 11680 98873 70817836
Folate deficiency 26.61 14.23 12 11723 3018 70913691
Dermatitis atopic 25.88 14.23 17 11718 8990 70907719
Resorption bone increased 24.27 14.23 9 11726 1376 70915333
Pain of skin 23.87 14.23 17 11718 10249 70906460
Odynophagia 21.72 14.23 16 11719 10159 70906550
Staphylococcal infection 20.68 14.23 34 11701 53370 70863339
Skin discolouration 20.52 14.23 28 11707 37297 70879412
Toxic epidermal necrolysis 19.26 14.23 28 11707 39529 70877180
Skin infection 19.05 14.23 18 11717 16094 70900615
Surgery 18.81 14.23 24 11711 29965 70886744
Pneumonia 18.71 14.23 165 11570 596067 70320642
Bronchial oedema 18.22 14.23 4 11731 90 70916619
Knee operation 18.20 14.23 11 11724 5036 70911673
Steroid withdrawal syndrome 17.65 14.23 6 11729 713 70915996
Skin exfoliation 17.55 14.23 30 11705 48596 70868113
Therapy interrupted 17.40 14.23 21 11714 24781 70891928
Drug interaction 16.96 14.23 23 11712 381418 70535291
Vestibular disorder 16.68 14.23 8 11727 2312 70914397
Skin cancer 15.77 14.23 15 11720 13521 70903188
Dry skin 15.75 14.23 31 11704 55900 70860809
Dermatitis contact 15.75 14.23 13 11722 9736 70906973
Otitis externa fungal 14.81 14.23 3 11732 45 70916664
Vertigo positional 14.66 14.23 8 11727 3025 70913684

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
ATC D06AX09 DERMATOLOGICALS
ANTIBIOTICS AND CHEMOTHERAPEUTICS FOR DERMATOLOGICAL USE
ANTIBIOTICS FOR TOPICAL USE
Other antibiotics for topical use
ATC R01AX06 RESPIRATORY SYSTEM
NASAL PREPARATIONS
DECONGESTANTS AND OTHER NASAL PREPARATIONS FOR TOPICAL USE
Other nasal preparations
FDA EPC N0000175515 RNA Synthetase Inhibitor Antibacterial
FDA MoA N0000175516 RNA Synthetase Inhibitors
CHEBI has role CHEBI:36047 antibacterial drugs
CHEBI has role CHEBI:48001 protein synthesis inhibitors
CHEBI has role CHEBI:35441 antiinfective agents
MeSH PA D000900 Anti-Bacterial Agents
MeSH PA D000890 Anti-Infective Agents
MeSH PA D004791 Enzyme Inhibitors
MeSH PA D011500 Protein Synthesis Inhibitors

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

DiseaseRelationSNOMED_IDDOID
Impetigo indication 48277006 DOID:8504
Staph Aureus Traumatic Skin Lesion Infection indication
Methicillin-Resistant Staphylococcus Aureus Nasal Colonization indication
Traumatic Skin Lesion Streptococcus Pyogenes Infection indication
Folliculitis off-label use 13600006 DOID:4409
Atopic dermatitis off-label use 24079001 DOID:3310
Eczema off-label use 43116000
Epidermolysis bullosa off-label use 61003004 DOID:2730
Ecthyma off-label use 85791004
Furunculosis off-label use 112650006
Minor Bacterial Skin Infections off-label use
Skin irritation contraindication 367466007




🐶 Veterinary Drug Use

SpeciesUseRelation
Dogs Bacterial infections of the skin caused by strains of Staphylococcus aureus Indication
Dogs Bacterial infections of the skin caused by Staphylococcus intermedius Indication

🐶 Veterinary products

ProductApplicantIngredients
Bactoderm Ointment Zoetis Inc. 1
Muricin Fougera Pharmaceuticals Inc. 1
Mupirocin Ointment USP, 2% Taro Pharmaceuticals U.S.A. Inc. 1

Acid dissociation constants calculated using MoKa v3.0.0

Dissociation levelDissociation constantType (acidic/basic)
pKa1 4.76 acidic
pKa2 12.42 acidic

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

Formulation strengthTrade nameApplicantApplication numberApproval dateTypeDose formRouteExclusivity dateDescription
EQ 2% BASE MUPIROCIN ALEOR DERMACEUTICALS A213053 Nov. 16, 2021 RX CREAM TOPICAL June 27, 2022 COMPETITIVE GENERIC THERAPY

Bioactivity Summary:

TargetClassPharosUniProtActionTypeActivity value
(-log[M])
Mechanism
action
Bioact sourceMoA source
Isoleucine--tRNA ligase, cytoplasmic Enzyme IC50 9.10 CHEMBL
Isoleucine--tRNA ligase Enzyme INHIBITOR DRUGBANK CHEMBL
Isoleucine--tRNA ligase Enzyme INHIBITOR CHEMBL CHEMBL
Isoleucine--tRNA ligase Enzyme Ki 8.60 CHEMBL
Isoleucine--tRNA ligase Enzyme Ki 7.22 CHEMBL
Isoleucine--tRNA ligase, putative, EC 6.1.1.5 Unclassified IC50 7.24 IUPHAR

External reference:

IDSource
4019345 VUID
N0000147519 NUI
D01076 KEGG_DRUG
115074-43-6 SECONDARY_CAS_RN
4019345 VANDF
4021018 VANDF
C0085259 UMLSCUI
CHEBI:7025 CHEBI
MRC PDB_CHEM_ID
CHEMBL3989715 ChEMBL_ID
CHEMBL2068726 ChEMBL_ID
CHEMBL719 ChEMBL_ID
D016712 MESH_DESCRIPTOR_UI
DB00410 DRUGBANK_ID
10916 IUPHAR_LIGAND_ID
5276 INN_ID
D0GX863OA5 UNII
446596 PUBCHEM_CID
221128 RXNORM
198973 MMSL
47751 MMSL
5138 MMSL
5139 MMSL
720 MMSL
002802 NDDF
005869 NDDF
387397004 SNOMEDCT_US
441528009 SNOMEDCT_US
71453003 SNOMEDCT_US

Pharmaceutical products:

ProductCategoryIngredientsNDCFormQuantityRouteMarketingLabel
Mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 0093-1010 OINTMENT 20 mg TOPICAL ANDA 23 sections
Mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 0168-0352 OINTMENT 20 mg TOPICAL ANDA 23 sections
BACTROBAN HUMAN PRESCRIPTION DRUG LABEL 1 16590-028 CREAM 20 mg TOPICAL NDA 22 sections
MUPIROCIN HUMAN PRESCRIPTION DRUG LABEL 1 16590-158 OINTMENT 20 mg TOPICAL ANDA 16 sections
Mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 16714-055 CREAM 20 mg TOPICAL ANDA 28 sections
mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 17856-0112 OINTMENT 20 mg TOPICAL ANDA 20 sections
Mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 21695-188 OINTMENT 20 mg TOPICAL ANDA 19 sections
Mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 21922-029 CREAM 2 g TOPICAL ANDA 23 sections
Mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 42254-137 OINTMENT 20 mg TOPICAL ANDA 19 sections
mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 42254-229 OINTMENT 20 mg TOPICAL ANDA 20 sections
CENTANY HUMAN PRESCRIPTION DRUG LABEL 1 43538-300 OINTMENT 20 mg TOPICAL NDA 26 sections
Centany AT HUMAN PRESCRIPTION DRUG LABEL 1 43538-310 OINTMENT 20 mg TOPICAL NDA 26 sections
MUPIROCIN HUMAN PRESCRIPTION DRUG LABEL 1 45802-018 CREAM 20 mg TOPICAL ANDA 25 sections
mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 45802-112 OINTMENT 20 mg TOPICAL ANDA 24 sections
mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 45802-112 OINTMENT 20 mg TOPICAL ANDA 24 sections
Mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 45865-722 OINTMENT 20 mg TOPICAL ANDA 20 sections
mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 49999-644 OINTMENT 20 mg TOPICAL ANDA 20 sections
mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 49999-644 OINTMENT 20 mg TOPICAL ANDA 20 sections
mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 50090-1587 OINTMENT 20 mg TOPICAL ANDA 24 sections
mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 50090-4349 OINTMENT 20 mg TOPICAL ANDA 24 sections
mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 50090-4397 OINTMENT 20 mg TOPICAL ANDA 24 sections
Mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 50268-568 OINTMENT 20 mg TOPICAL ANDA 25 sections
Mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 50436-0025 OINTMENT 20 mg TOPICAL ANDA 23 sections
mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 50436-0112 OINTMENT 20 mg TOPICAL ANDA 24 sections
Mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 50436-0180 OINTMENT 20 mg TOPICAL ANDA 22 sections
Mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 50436-1010 OINTMENT 20 mg TOPICAL ANDA 23 sections
Mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 51672-1312 OINTMENT 20 mg TOPICAL ANDA 25 sections
Mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 51672-1370 CREAM 20 mg TOPICAL ANDA 28 sections
mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 52959-743 OINTMENT 20 mg TOPICAL ANDA 20 sections
Mupirocin HUMAN PRESCRIPTION DRUG LABEL 1 53002-9850 OINTMENT 20 mg TOPICAL ANDA 22 sections