Home > National Drug Code (NDC) > MEDROXYPROGESTERONE ACETATE

MEDROXYPROGESTERONE ACETATE - 54868-0109-0 - (medroxyprogesterone acetate)

Alphabetical Index


Drug Information of MEDROXYPROGESTERONE ACETATE

Product NDC: 54868-0109
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: 54868-0109
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011839
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19940706

Package Information of MEDROXYPROGESTERONE ACETATE

Package NDC: 54868-0109-0
Package Description: 25 TABLET in 1 BOTTLE, PLASTIC (54868-0109-0)

NDC Information of MEDROXYPROGESTERONE ACETATE

NDC Code 54868-0109-0
Proprietary Name MEDROXYPROGESTERONE ACETATE
Package Description 25 TABLET in 1 BOTTLE, PLASTIC (54868-0109-0)
Product NDC 54868-0109
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name medroxyprogesterone acetate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19940706
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Physicians Total Care, 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


General Information