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Medroxyprogesterone Acetate - 55289-160-07 - (Medroxyprogesterone Acetate)

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Drug Information of Medroxyprogesterone Acetate

Product NDC: 55289-160
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: 55289-160
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040159
Marketing Category: ANDA
Start Marketing Date: 20110118

Package Information of Medroxyprogesterone Acetate

Package NDC: 55289-160-07
Package Description: 7 TABLET in 1 BOTTLE, PLASTIC (55289-160-07)

NDC Information of Medroxyprogesterone Acetate

NDC Code 55289-160-07
Proprietary Name Medroxyprogesterone Acetate
Package Description 7 TABLET in 1 BOTTLE, PLASTIC (55289-160-07)
Product NDC 55289-160
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Medroxyprogesterone Acetate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110118
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
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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