Home > National Drug Code (NDC) > Megestrol Acetate

Megestrol Acetate - 54868-1629-3 - (Megestrol Acetate)

Alphabetical Index


Drug Information of Megestrol Acetate

Product NDC: 54868-1629
Proprietary Name: Megestrol Acetate
Non Proprietary Name: Megestrol Acetate
Active Ingredient(s): 40    mg/1 & nbsp;   Megestrol Acetate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Megestrol Acetate

Product NDC: 54868-1629
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072423
Marketing Category: ANDA
Start Marketing Date: 20070705

Package Information of Megestrol Acetate

Package NDC: 54868-1629-3
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (54868-1629-3)

NDC Information of Megestrol Acetate

NDC Code 54868-1629-3
Proprietary Name Megestrol Acetate
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (54868-1629-3)
Product NDC 54868-1629
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Megestrol Acetate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070705
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name MEGESTROL ACETATE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Progesterone Congeners [Chemical/Ingredient],Progestin [EPC]

Complete Information of Megestrol Acetate


General Information