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Lupron Depot-PED - 0074-2108-03 - (leuprolide acetate)

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Drug Information of Lupron Depot-PED

Product NDC: 0074-2108
Proprietary Name: Lupron Depot-PED
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-PED

Product NDC: 0074-2108
Labeler Name: AbbVie Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020263
Marketing Category: NDA
Start Marketing Date: 19930416

Package Information of Lupron Depot-PED

Package NDC: 0074-2108-03
Package Description: 1 KIT in 1 CARTON (0074-2108-03) * 1 mL in 1 SYRINGE * 1 SWAB in 1 PACKET

NDC Information of Lupron Depot-PED

NDC Code 0074-2108-03
Proprietary Name Lupron Depot-PED
Package Description 1 KIT in 1 CARTON (0074-2108-03) * 1 mL in 1 SYRINGE * 1 SWAB in 1 PACKET
Product NDC 0074-2108
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name leuprolide acetate
Dosage Form Name KIT
Route Name
Start Marketing Date 19930416
Marketing Category Name NDA
Labeler Name AbbVie Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Lupron Depot-PED


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