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Medroxyprogesterone Acetate - 63629-2612-3 - (Medroxyprogesterone Acetate)

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Drug Information of Medroxyprogesterone Acetate

Product NDC: 63629-2612
Proprietary Name: Medroxyprogesterone Acetate
Non Proprietary Name: Medroxyprogesterone Acetate
Active Ingredient(s): 10    mg/1 & nbsp;   Medroxyprogesterone Acetate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Medroxyprogesterone Acetate

Product NDC: 63629-2612
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040159
Marketing Category: ANDA
Start Marketing Date: 19961204

Package Information of Medroxyprogesterone Acetate

Package NDC: 63629-2612-3
Package Description: 5 TABLET in 1 BOTTLE (63629-2612-3)

NDC Information of Medroxyprogesterone Acetate

NDC Code 63629-2612-3
Proprietary Name Medroxyprogesterone Acetate
Package Description 5 TABLET in 1 BOTTLE (63629-2612-3)
Product NDC 63629-2612
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Medroxyprogesterone Acetate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19961204
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name MEDROXYPROGESTERONE ACETATE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Progesterone Congeners [Chemical/Ingredient],Progestin [EPC]

Complete Information of Medroxyprogesterone Acetate


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