mupirocin

Product NDC
63629-8687
11-digit product format
636298687
Labeler code
63629
Product ID
63629-8687_228603d0-e8ef-4769-8e79-3c7bbc6c88c4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Mupirocin
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Bryant Ranch Prepack
Application
ANDA065123
Marketing category
ANDA
Marketing start
2009-10-30
Substance
MUPIROCIN
Active strength
20 mg/g
Pharmacologic classes
RNA Synthetase Inhibitor Antibacterial [EPC], RNA Synthetase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data

Finished product
Yes
Brand name base
mupirocin
Listing expiration
2026-12-31

Related Records

Active Ingredients

IngredientStrength
MUPIROCIN20 mg/g

Harmonized Identifiers

FieldValues
UniiD0GX863OA5
Rxcui106346

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
D0GX863OA5MUPIROCIN12650-69-0MUPIROCIN

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-8687-1636298687011 TUBE in 1 CARTON (63629-8687-1) / 22 g in 1 TUBE1 tube2021-07-210000-00-00NoNoCurrent

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
mupirocinBryant Ranch Prepack2023-07-18HUMAN PRESCRIPTION DRUG LABEL105