BACTROBAN - 16590-028-30 - (MUPIROCIN CALCIUM)

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Drug Information of BACTROBAN

Product NDC: 16590-028
Proprietary Name: BACTROBAN
Non Proprietary Name: MUPIROCIN CALCIUM
Active Ingredient(s): 20    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: 16590-028
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050746
Marketing Category: NDA
Start Marketing Date: 19980123

Package Information of BACTROBAN

Package NDC: 16590-028-30
Package Description: 30 g in 1 TUBE (16590-028-30)

NDC Information of BACTROBAN

NDC Code 16590-028-30
Proprietary Name BACTROBAN
Package Description 30 g in 1 TUBE (16590-028-30)
Product NDC 16590-028
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 STAT RX USA LLC
Substance Name MUPIROCIN CALCIUM
Strength Number 20
Strength Unit mg/g
Pharmaceutical Classes RNA Synthetase Inhibitor Antibacterial [EPC],RNA Synthetase Inhibitors [MoA]

Complete Information of BACTROBAN


General Information