Megestrol Acetate
Megestrol Acetate Oral Suspension
Approved
Approval ID
95dfc24a-5744-4ddf-8809-86184142a372
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 18, 2023
Manufacturers
FDA
McKesson Corporation dba SKY Packaging
DUNS: 140529962
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 Code63739-549
Application NumberANDA075671
Product Classification
M
Marketing Category
C73584
G
Generic Name
Megestrol Acetate
Product Specifications
Route of AdministrationORAL
Effective DateDecember 18, 2023
FDA Product Classification
INGREDIENTS (1)
MEGESTROL ACETATEActive
Quantity: 400 mg in 10 mL
Code: TJ2M0FR8ES
Classification: ACTIB