Mupirocin (Page 4 of 4)

PACKAGE/LABEL PRINCIPAL DISPLAY PANEL

Rx Only

Mupirocin Ointment USP, 2%

NET WT 22 g

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MUPIROCIN
mupirocin ointment
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:76420-128(NDC:45802-112)
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, UNSPECIFIED
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:76420-128-22 22 g in 1 TUBE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA065123 10/30/2009
Labeler — Asclemed USA, Inc. (059888437)
Establishment
Name Address ID/FEI Operations
ASCLEMED USA INC. DBA ENOVACHEM 059888437 relabel (76420-128)

Revised: 11/2020 Asclemed USA, Inc.

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