Mupirocin - 51672-1312-0 - (Mupirocin)

Alphabetical Index


Drug Information of Mupirocin

Product NDC: 51672-1312
Proprietary Name: Mupirocin
Non Proprietary Name: Mupirocin
Active Ingredient(s): 20    mg/g & nbsp;   Mupirocin
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Mupirocin

Product NDC: 51672-1312
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065170
Marketing Category: ANDA
Start Marketing Date: 20050923

Package Information of Mupirocin

Package NDC: 51672-1312-0
Package Description: 1 TUBE in 1 CARTON (51672-1312-0) > 22 g in 1 TUBE

NDC Information of Mupirocin

NDC Code 51672-1312-0
Proprietary Name Mupirocin
Package Description 1 TUBE in 1 CARTON (51672-1312-0) > 22 g in 1 TUBE
Product NDC 51672-1312
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mupirocin
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20050923
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name MUPIROCIN
Strength Number 20
Strength Unit mg/g
Pharmaceutical Classes RNA Synthetase Inhibitor Antibacterial [EPC],RNA Synthetase Inhibitors [MoA]

Complete Information of Mupirocin


General Information