NDC 68462-180-22
API & Excipient Details

Mupirocin marketed by Glenmark Pharmaceuticals Inc., USA under NDC Code 68462-180-22

NDC Code(s) : 68462-180-22
Packager : Glenmark Pharmaceuticals Inc., USA

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

MupirocinMupirocin OINTMENT

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC:68462-180
Route of Administration	TOPICAL	DEA Schedule

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
MUPIROCIN(UNII: D0GX863OA5) (MUPIROCIN - UNII:D0GX863OA5)	MUPIROCIN	20 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
POLYETHYLENE GLYCOL 400(UNII: B697894SGQ)
POLYETHYLENE GLYCOL 3350(UNII: G2M7P15E5P)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:68462-180-22	22 g in 1 TUBE Type 0: Not a Combination Product	06/08/2011

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
ANDA	ANDA090480	06/08/2011

LABELER - Glenmark Pharmaceuticals Inc., USA(130597813)

Establishment
Name	Address	ID/FEI	Business Operations
Glenmark Pharmaceuticals Ltd		677318665	MANUFACTURE(68462-180), ANALYSIS(68462-180)

PRINCIPAL DISPLAY PANEL

NDC 68462-180-22

Mupirocin Ointment USP, 2% - 22 g