Megestrol Acetate
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Approved
Approval ID
239dacec-8c96-4f4d-878a-b9681cb390f3
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 20, 2021
Manufacturers
FDA
ATLANTIC BIOLOGICALS CORP.
DUNS: 047437707
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 Code17856-0907
Application NumberANDA075671
Product Classification
M
Marketing Category
C73584
G
Generic Name
Megestrol Acetate
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 18, 2021
FDA Product Classification
INGREDIENTS (1)
MEGESTROL ACETATEActive
Quantity: 40 mg in 1 mL
Code: TJ2M0FR8ES
Classification: ACTIB