Megestrol Acetate
{'@ID': 'inv-da1ad2f6-f8ce-4fd6-b830-23f778e6926e'}
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
NDC Product Code17856-0907
Application NumberANDA075671
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateJanuary 18, 2021
Generic NameMegestrol Acetate
INGREDIENTS (1)
MEGESTROL ACETATEActive
Quantity: 40 mg in 1 mL
Code: TJ2M0FR8ES
Classification: ACTIB