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Megestrol Acetate - 49884-289-01 - (Megestrol Acetate)

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Drug Information of Megestrol Acetate

Product NDC: 49884-289
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: 49884-289
Labeler Name: Par Pharmaceutical Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072422
Marketing Category: ANDA
Start Marketing Date: 19880808

Package Information of Megestrol Acetate

Package NDC: 49884-289-01
Package Description: 100 TABLET in 1 BOTTLE (49884-289-01)

NDC Information of Megestrol Acetate

NDC Code 49884-289-01
Proprietary Name Megestrol Acetate
Package Description 100 TABLET in 1 BOTTLE (49884-289-01)
Product NDC 49884-289
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Megestrol Acetate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19880808
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical 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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