Mupirocin (Page 4 of 4)

MUPIROCIN OINTMENT

Label Image
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MUPIROCIN
mupirocin ointment
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50436-0025(NDC:0168-0352)
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUPIROCIN (MUPIROCIN) MUPIROCIN 20 mg in 1 g
Inactive Ingredients
Ingredient Name Strength
POLYETHYLENE GLYCOL 3350
POLYETHYLENE GLYCOL 400
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50436-0025-1 22 g in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA065192 11/30/2005
Labeler — Unit Dose Services (831995316)
Establishment
Name Address ID/FEI Operations
Unit Dose Services 831995316 REPACK (50436-0025), RELABEL (50436-0025)

Revised: 08/2021 Unit Dose Services

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