Mupirocin

Mupirocin

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

Company

DUNS: 079674019

Effective Date

April 16, 2018

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

Central Texas Community Health Centers

DUNS Number

797039398

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

NDC Product Code

76413-158

Application Number

ANDA090480

Marketing Category

ANDA (C73584)

Route of Administration

TOPICAL

Effective Date

July 12, 2017

Ingredients

POLYETHYLENE GLYCOL 400Inactive

Code: B697894SGQClass: IACT

Code: D0GX863OA5Class: ACTIBQuantity: 20 mg in 1 g

POLYETHYLENE GLYCOL 3350Inactive

Code: G2M7P15E5PClass: IACT