Megestrol Acetate

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

Company

DUNS: 603184490

Effective Date

August 15, 2023

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Manufacturing Establishments1

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

Labeler

Golden State Medical Supply, Inc.

DUNS Number

603184490

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

NDC Product Code

60429-433

Application Number

ANDA072423

Marketing Category

ANDA (C73584)

Route of Administration

ORAL

Effective Date

August 15, 2023

Ingredients

Code: TJ2M0FR8ESClass: ACTIBQuantity: 40 mg in 1 1