mupirocin

mupirocin

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

Company

DUNS: 830016429

Effective Date

May 25, 2021

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Mupirocin(20 mg in 1 g)

Manufacturing Establishments1

FDA-registered manufacturing facilities and establishments involved in the production, packaging, or distribution of this drug product.

Labeler

A-S Medication Solutions

DUNS Number

830016429

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

NDC Product Code

50090-4349

Application Number

ANDA065123

Marketing Category

ANDA (C73584)

Route of Administration

TOPICAL

Effective Date

December 9, 2019

Ingredients

POLYETHYLENE GLYCOL, UNSPECIFIEDInactive

Code: 3WJQ0SDW1AClass: IACT

Code: D0GX863OA5Class: ACTIBQuantity: 20 mg in 1 g