Megace ES
MEGACE ES (megestrol acetate oral suspension) suspension
Approved
Approval ID
33bc102c-31a3-4fd9-9702-c1193d7699a3
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 27, 2009
Manufacturers
FDA
Stat Rx USA
DUNS: 786036330
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 Code16590-254
Application NumberNDA021778
Product Classification
M
Marketing Category
C73594
G
Generic Name
MEGESTROL ACETATE
Product Specifications
Route of AdministrationORAL
Effective DateOctober 27, 2009
FDA Product Classification
INGREDIENTS (1)
MEGESTROL ACETATEActive
Quantity: 125 mg in 1 mL
Code: TJ2M0FR8ES
Classification: ACTIB