Mupirocin - 68462-564-17 - (Mupirocin)

Alphabetical Index


Drug Information of Mupirocin

Product NDC: 68462-564
Proprietary Name: Mupirocin
Non Proprietary Name: Mupirocin
Active Ingredient(s): 2    g/100g & nbsp;   Mupirocin
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Mupirocin

Product NDC: 68462-564
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201587
Marketing Category: ANDA
Start Marketing Date: 20130124

Package Information of Mupirocin

Package NDC: 68462-564-17
Package Description: 15 g in 1 TUBE (68462-564-17)

NDC Information of Mupirocin

NDC Code 68462-564-17
Proprietary Name Mupirocin
Package Description 15 g in 1 TUBE (68462-564-17)
Product NDC 68462-564
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mupirocin
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20130124
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc., USA
Substance Name MUPIROCIN CALCIUM
Strength Number 2
Strength Unit g/100g
Pharmaceutical Classes RNA Synthetase Inhibitor Antibacterial [EPC],RNA Synthetase Inhibitors [MoA]

Complete Information of Mupirocin


General Information