NDC 17033-273 - Mometavet

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
17033-273
Package NDCs from labels
17033-273-75, 17033-273-15, 17033-273-30, 17033-273-21
Manufacturer
Dechra Veterinary Products, LLC
Effective date
2024-02-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Mometavet - Dechra Veterinary Products, LLCDechra Veterinary Products, LLC2024-02-21PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17033-273-15Mometavet15 g in 1 BOTTLE, PLASTICSUSPENSION151
17033-273-21Mometavet215 g in 1 BOTTLE, PLASTICSUSPENSION2151
17033-273-30Mometavet30 g in 1 BOTTLE, PLASTICSUSPENSION301
17033-273-75Mometavet7.5 g in 1 BOTTLE, PLASTICSUSPENSION7.51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17033-273MOMETAVET (GENTAMICIN SULFATE, MOMETASONE FUROATE ANHYDROUS, AND CLOTRIMAZOLE) SUSPENSION [DECHRA VETERINARY PRODUCTS, LLC]14 package rows20240223_f92c6521-4912-4796-bed5-7a1694984e04.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 16 of 16 · 314 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Gentamicin SulfateGENTAMICIN SULFATEAsclemed USA, Inc.a54e5c95-609d-4d66-9573-5d1ac78fa58f2022-03-04Warnings, Adverse reactionsExact identifier
unii: 8X7386QRLV
Micomitin AntifungalCLOTRIMAZOLEPureTek Corporationdd05f5f9-2412-1295-e053-2995a90acb962022-02-14WarningsExact identifier
unii: G07GZ97H65
ClotrimazoleCLOTRIMAZOLEProficient Rx LPc62264a9-cea3-4461-9399-35d8931d38d52022-02-01Warnings, Adverse reactionsExact identifier
unii: G07GZ97H65
ClotrimazoleCLOTRIMAZOLEHikma Pharmacuticals USA USA Inc.0bc4b876-ddee-4f03-b44f-544348739a262021-07-30Warnings, Adverse reactionsExact identifier
unii: G07GZ97H65
Gentamicin SulfateGENTAMICIN SULFATEProficient Rx LPcf4386ba-c62a-4ee8-ab59-1bb2e737a5da2021-05-01Adverse reactionsExact identifier
unii: 8X7386QRLV
Mometasone FuroateMOMETASONE FUROATEProficient Rx LP47a60763-671e-413b-b962-f7f11ba2f4d72021-01-01Warnings, Adverse reactionsExact identifier
unii: 04201GDN4R
Clotrimazole and Betamethasone DipropionateCLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATEProficient Rx LPc6e4bf5f-f6d6-489e-9286-c30568c601b72021-01-01Warnings, Adverse reactionsExact identifier
unii: G07GZ97H65
Clotrimazole and Betamethasone DipropionateCLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATEGlenmark Pharmaceuticals Inc. USA8dcd24cb-e568-428a-88ac-737d115cc54d2020-11-09Warnings, Adverse reactionsExact identifier
unii: G07GZ97H65
ClotrimazoleCLOTRIMAZOLE TOPICALNovitium Pharma LLC02df90b9-4879-4e73-b03a-0e96f3d099ea2020-08-13Warnings, Adverse reactionsExact identifier
unii: G07GZ97H65
Mometasone FuroateMOMETASONE FUROATEGlenmark Pharmaceuticals Inc., USA96eafc06-0354-49ca-a684-a77bb2afc8f52020-05-31Warnings, Adverse reactionsExact identifier
unii: 04201GDN4R
Mometasone FuroateMOMETASONE FUROATEProficient Rx LPc08fcb0d-7fff-4d90-aeb8-e912b930bf3d2020-02-01Warnings, Adverse reactionsExact identifier
unii: 04201GDN4R
GentakGENTAMICIN SULFATEProficient Rx LPaebfe247-cdf7-4acb-97b3-6d4341d7c8152019-11-01Warnings, Adverse reactionsExact identifier
unii: 8X7386QRLV
Gentamicin SulfateGENTAMICIN SULFATEProficient Rx LP2098faaa-7f60-4640-8c37-19456ebba6532019-11-01Warnings, Adverse reactionsExact identifier
unii: 8X7386QRLV
Mometasone FuroateMOMETASONE FUROATEGlenmark Pharmaceuticals Inc., USA031283ed-988b-4698-8a2e-00f3d41c0f712019-07-09Warnings, Adverse reactionsExact identifier
unii: 04201GDN4R

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.