Mupirocin

Mupirocin

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

Company

DUNS: 118802834

Effective Date

October 6, 2010

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

Rebel Distributors Corp.

DUNS Number

118802834

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

NDC Product Code

21695-188

Application Number

ANDA065192

Marketing Category

ANDA (C73584)

Route of Administration

TOPICAL

Effective Date

November 11, 2009

Ingredients

Code: D0GX863OA5Class: ACTIBQuantity: 20 mg in 1 g

polyethylene glycol 400Inactive

Code: B697894SGQClass: IACT

polyethylene glycol 3350Inactive

Code: G2M7P15E5PClass: IACT