Mupirocin - 54868-4958-0 - (mupirocin)

Alphabetical Index


Drug Information of Mupirocin

Product NDC: 54868-4958
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: 54868-4958
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065192
Marketing Category: ANDA
Start Marketing Date: 20031205

Package Information of Mupirocin

Package NDC: 54868-4958-0
Package Description: 1 TUBE in 1 CARTON (54868-4958-0) > 22 g in 1 TUBE

NDC Information of Mupirocin

NDC Code 54868-4958-0
Proprietary Name Mupirocin
Package Description 1 TUBE in 1 CARTON (54868-4958-0) > 22 g in 1 TUBE
Product NDC 54868-4958
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name mupirocin
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20031205
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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