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Depo-Provera - 0009-7376-11 - (medroxyprogesterone acetate)

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Drug Information of Depo-Provera

Product NDC: 0009-7376
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: 0009-7376
Labeler Name: Pharmacia and Upjohn Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020246
Marketing Category: NDA
Start Marketing Date: 19921029

Package Information of Depo-Provera

Package NDC: 0009-7376-11
Package Description: 1 mL in 1 SYRINGE (0009-7376-11)

NDC Information of Depo-Provera

NDC Code 0009-7376-11
Proprietary Name Depo-Provera
Package Description 1 mL in 1 SYRINGE (0009-7376-11)
Product NDC 0009-7376
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name medroxyprogesterone acetate
Dosage Form Name INJECTION, SUSPENSION
Route Name INTRAMUSCULAR
Start Marketing Date 19921029
Marketing Category Name NDA
Labeler Name Pharmacia and Upjohn Company
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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