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Lupron Depot - 0074-3641-71 - (leuprolide acetate)

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Drug Information of Lupron Depot

Product NDC: 0074-3641
Proprietary Name: Lupron Depot
Non Proprietary Name: leuprolide acetate
Active Ingredient(s):    & nbsp;   leuprolide acetate
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Lupron Depot

Product NDC: 0074-3641
Labeler Name: Abbott Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020011
Marketing Category: NDA
Start Marketing Date: 19901022

Package Information of Lupron Depot

Package NDC: 0074-3641-71
Package Description: 1 KIT in 1 CARTON * 1 mL in 1 SYRINGE * 1 mL in 1 PACKET

NDC Information of Lupron Depot

NDC Code 0074-3641-71
Proprietary Name Lupron Depot
Package Description 1 KIT in 1 CARTON * 1 mL in 1 SYRINGE * 1 mL in 1 PACKET
Product NDC 0074-3641
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name leuprolide acetate
Dosage Form Name KIT
Route Name
Start Marketing Date 19901022
Marketing Category Name NDA
Labeler Name Abbott Laboratories
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Lupron Depot


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