mupirocin - 45802-112-22 - (Mupirocin)

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Drug Information of mupirocin

Product NDC: 45802-112
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: 45802-112
Labeler Name: Perrigo New York Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065123
Marketing Category: ANDA
Start Marketing Date: 20091030

Package Information of mupirocin

Package NDC: 45802-112-22
Package Description: 1 TUBE in 1 CARTON (45802-112-22) > 22 g in 1 TUBE

NDC Information of mupirocin

NDC Code 45802-112-22
Proprietary Name mupirocin
Package Description 1 TUBE in 1 CARTON (45802-112-22) > 22 g in 1 TUBE
Product NDC 45802-112
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mupirocin
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20091030
Marketing Category Name ANDA
Labeler Name Perrigo New York 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