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Megestrol Acetate - 0054-4603-25 - (Megestrol Acetate)

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Drug Information of Megestrol Acetate

Product NDC: 0054-4603
Proprietary Name: Megestrol Acetate
Non Proprietary Name: Megestrol Acetate
Active Ingredient(s): 20    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: 0054-4603
Labeler Name: Roxane Laboratories, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074458
Marketing Category: ANDA
Start Marketing Date: 19950929

Package Information of Megestrol Acetate

Package NDC: 0054-4603-25
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0054-4603-25)

NDC Information of Megestrol Acetate

NDC Code 0054-4603-25
Proprietary Name Megestrol Acetate
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0054-4603-25)
Product NDC 0054-4603
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Megestrol Acetate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19950929
Marketing Category Name ANDA
Labeler Name Roxane Laboratories, Inc
Substance Name MEGESTROL ACETATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Progesterone Congeners [Chemical/Ingredient],Progestin [EPC]

Complete Information of Megestrol Acetate


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