Provera - 0009-0050-11 - (medroxyprogesterone acetate)

Alphabetical Index


Drug Information of Provera

Product NDC: 0009-0050
Proprietary Name: Provera
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 Provera

Product NDC: 0009-0050
Labeler Name: Pharmacia and Upjohn Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011839
Marketing Category: NDA
Start Marketing Date: 19590603

Package Information of Provera

Package NDC: 0009-0050-11
Package Description: 500 TABLET in 1 BOTTLE (0009-0050-11)

NDC Information of Provera

NDC Code 0009-0050-11
Proprietary Name Provera
Package Description 500 TABLET in 1 BOTTLE (0009-0050-11)
Product NDC 0009-0050
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
Labeler Name Pharmacia and Upjohn Company
Substance Name MEDROXYPROGESTERONE ACETATE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Progesterone Congeners [Chemical/Ingredient],Progestin [EPC]

Complete Information of Provera


General Information