MedPath

MEGESTOL

Approved
Approval ID

dd332944-d610-4338-9e5e-9b2e5e90e399

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jan 22, 2010

Manufacturers
FDA

STAT RX USA LLC

DUNS: 786036330

Products 1

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

MEGESTROL ACETATE

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code16590-898
Application NumberANDA075997
Product Classification
M
Marketing Category
C73584
G
Generic Name
MEGESTROL ACETATE
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 22, 2010
FDA Product Classification

INGREDIENTS (1)

MEGESTROL ACETATEActive
Quantity: 40 mg in 1 mL
Code: TJ2M0FR8ES
Classification: ACTIB

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.