Megestrol Acetate
Megestrol Acetate Tablet USP
Approved
Approval ID
4f94daf8-ceb9-4577-ab71-8b7e3db7ff8e
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 3, 2022
Manufacturers
FDA
Par Pharmaceutical, Inc.
DUNS: 092733690
Products 2
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 Code49884-290
Application NumberANDA072423
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateMay 3, 2022
Generic NameMegestrol Acetate
INGREDIENTS (1)
MEGESTROL ACETATEActive
Quantity: 40 mg in 1 1
Code: TJ2M0FR8ES
Classification: ACTIB
Megestrol Acetate
PRODUCT DETAILS
NDC Product Code49884-289
Application NumberANDA072422
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateMay 3, 2022
Generic NameMegestrol Acetate
INGREDIENTS (1)
MEGESTROL ACETATEActive
Quantity: 20 mg in 1 1
Code: TJ2M0FR8ES
Classification: ACTIB