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Medroxyprogesterone Acetate - 0555-0873-02 - (Medroxyprogesterone Acetate)

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Drug Information of Medroxyprogesterone Acetate

Product NDC: 0555-0873
Proprietary Name: Medroxyprogesterone Acetate
Non Proprietary Name: Medroxyprogesterone Acetate
Active Ingredient(s): 5    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: 0555-0873
Labeler Name: Barr Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040159
Marketing Category: ANDA
Start Marketing Date: 19961203

Package Information of Medroxyprogesterone Acetate

Package NDC: 0555-0873-02
Package Description: 100 TABLET in 1 BOTTLE (0555-0873-02)

NDC Information of Medroxyprogesterone Acetate

NDC Code 0555-0873-02
Proprietary Name Medroxyprogesterone Acetate
Package Description 100 TABLET in 1 BOTTLE (0555-0873-02)
Product NDC 0555-0873
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Medroxyprogesterone Acetate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19961203
Marketing Category Name ANDA
Labeler Name Barr Laboratories Inc.
Substance Name MEDROXYPROGESTERONE ACETATE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Progesterone Congeners [Chemical/Ingredient],Progestin [EPC]

Complete Information of Medroxyprogesterone Acetate


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