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medroxyprogesterone acetate - 59762-3742-6 - (MEDROXYPROGESTERONE ACETATE)

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Drug Information of medroxyprogesterone acetate

Product NDC: 59762-3742
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: 59762-3742
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011839
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19590603

Package Information of medroxyprogesterone acetate

Package NDC: 59762-3742-6
Package Description: 50 TABLET in 1 BOTTLE (59762-3742-6)

NDC Information of medroxyprogesterone acetate

NDC Code 59762-3742-6
Proprietary Name medroxyprogesterone acetate
Package Description 50 TABLET in 1 BOTTLE (59762-3742-6)
Product NDC 59762-3742
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MEDROXYPROGESTERONE ACETATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19590603
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone LLC
Substance Name MEDROXYPROGESTERONE ACETATE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Progesterone Congeners [Chemical/Ingredient],Progestin [EPC]

Complete Information of medroxyprogesterone acetate


General Information