Mupirocin

Mupirocin

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

Company

DUNS: 010632300

Effective Date

July 19, 2022

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

NuCare Pharmaceuticals,Inc.

DUNS Number

010632300

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

NDC Product Code

68071-4111

Application Number

ANDA090480

Marketing Category

ANDA (C73584)

Route of Administration

TOPICAL

Effective Date

July 19, 2022

Ingredients

POLYETHYLENE GLYCOL 3350Inactive

Code: G2M7P15E5PClass: IACT

POLYETHYLENE GLYCOL 400Inactive

Code: B697894SGQClass: IACT

Code: D0GX863OA5Class: ACTIBQuantity: 20 mg in 1 g