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Depo-Provera - 54868-4100-1 - (medroxyprogesterone acetate)

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Drug Information of Depo-Provera

Product NDC: 54868-4100
Proprietary Name: Depo-Provera
Non Proprietary Name: medroxyprogesterone acetate
Active Ingredient(s): 150    mg/mL & nbsp;   medroxyprogesterone acetate
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION, SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Depo-Provera

Product NDC: 54868-4100
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020246
Marketing Category: NDA
Start Marketing Date: 19990630

Package Information of Depo-Provera

Package NDC: 54868-4100-1
Package Description: 1 SYRINGE in 1 BOTTLE, DISPENSING (54868-4100-1) > 1 mL in 1 SYRINGE

NDC Information of Depo-Provera

NDC Code 54868-4100-1
Proprietary Name Depo-Provera
Package Description 1 SYRINGE in 1 BOTTLE, DISPENSING (54868-4100-1) > 1 mL in 1 SYRINGE
Product NDC 54868-4100
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name medroxyprogesterone acetate
Dosage Form Name INJECTION, SUSPENSION
Route Name INTRAMUSCULAR
Start Marketing Date 19990630
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name MEDROXYPROGESTERONE ACETATE
Strength Number 150
Strength Unit mg/mL
Pharmaceutical Classes Progesterone Congeners [Chemical/Ingredient],Progestin [EPC]

Complete Information of Depo-Provera


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