BACTROBAN - 0029-1527-22 - (mupirocin calcium)

Alphabetical Index


Drug Information of BACTROBAN

Product NDC: 0029-1527
Proprietary Name: BACTROBAN
Non Proprietary Name: mupirocin calcium
Active Ingredient(s): 21.5    mg/g & nbsp;   mupirocin calcium
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of BACTROBAN

Product NDC: 0029-1527
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050746
Marketing Category: NDA
Start Marketing Date: 19980123

Package Information of BACTROBAN

Package NDC: 0029-1527-22
Package Description: 1 TUBE in 1 CARTON (0029-1527-22) > 15 g in 1 TUBE

NDC Information of BACTROBAN

NDC Code 0029-1527-22
Proprietary Name BACTROBAN
Package Description 1 TUBE in 1 CARTON (0029-1527-22) > 15 g in 1 TUBE
Product NDC 0029-1527
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name mupirocin calcium
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19980123
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name MUPIROCIN CALCIUM
Strength Number 21.5
Strength Unit mg/g
Pharmaceutical Classes RNA Synthetase Inhibitor Antibacterial [EPC],RNA Synthetase Inhibitors [MoA]

Complete Information of BACTROBAN


General Information