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Depo-Provera - 54868-3613-0 - (medroxyprogesterone acetate)

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Drug Information of Depo-Provera

Product NDC: 54868-3613
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: 54868-3613
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020246
Marketing Category: NDA
Start Marketing Date: 20000124

Package Information of Depo-Provera

Package NDC: 54868-3613-0
Package Description: 1 VIAL in 1 BOTTLE, DISPENSING (54868-3613-0) > 1 mL in 1 VIAL

NDC Information of Depo-Provera

NDC Code 54868-3613-0
Proprietary Name Depo-Provera
Package Description 1 VIAL in 1 BOTTLE, DISPENSING (54868-3613-0) > 1 mL in 1 VIAL
Product NDC 54868-3613
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name medroxyprogesterone acetate
Dosage Form Name INJECTION, SUSPENSION
Route Name INTRAMUSCULAR
Start Marketing Date 20000124
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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