MUPIROCIN - 16590-158-22 - (MUPIROCIN)

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Drug Information of MUPIROCIN

Product NDC: 16590-158
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: 16590-158
Labeler Name: STAT RX LLC USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065123
Marketing Category: ANDA
Start Marketing Date: 20031107

Package Information of MUPIROCIN

Package NDC: 16590-158-22
Package Description: 22 g in 1 TUBE (16590-158-22)

NDC Information of MUPIROCIN

NDC Code 16590-158-22
Proprietary Name MUPIROCIN
Package Description 22 g in 1 TUBE (16590-158-22)
Product NDC 16590-158
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MUPIROCIN
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20031107
Marketing Category Name ANDA
Labeler Name STAT RX LLC USA
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