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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code49884-290
Application NumberANDA072423
Product Classification
M
Marketing Category
C73584
G
Generic Name
Megestrol Acetate
Product Specifications
Route of AdministrationORAL
Effective DateMay 3, 2022
FDA Product Classification
INGREDIENTS (1)
MEGESTROL ACETATEActive
Quantity: 40 mg in 1 1
Code: TJ2M0FR8ES
Classification: ACTIB
Megestrol Acetate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code49884-289
Application NumberANDA072422
Product Classification
M
Marketing Category
C73584
G
Generic Name
Megestrol Acetate
Product Specifications
Route of AdministrationORAL
Effective DateMay 3, 2022
FDA Product Classification
INGREDIENTS (1)
MEGESTROL ACETATEActive
Quantity: 20 mg in 1 1
Code: TJ2M0FR8ES
Classification: ACTIB