VIVITROL - 65757-301-01 - (naltrexone)

Alphabetical Index


Drug Information of VIVITROL

Product NDC: 65757-301
Proprietary Name: VIVITROL
Non Proprietary Name: naltrexone
Active Ingredient(s):    & nbsp;   naltrexone
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of VIVITROL

Product NDC: 65757-301
Labeler Name: Alkermes, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021897
Marketing Category: NDA
Start Marketing Date: 20060613

Package Information of VIVITROL

Package NDC: 65757-301-01
Package Description: 1 KIT in 1 CARTON (65757-301-01) * 4 mL in 1 VIAL, GLASS (65757-303-02) * 4 mL in 1 VIAL, GLASS (65757-305-03)

NDC Information of VIVITROL

NDC Code 65757-301-01
Proprietary Name VIVITROL
Package Description 1 KIT in 1 CARTON (65757-301-01) * 4 mL in 1 VIAL, GLASS (65757-303-02) * 4 mL in 1 VIAL, GLASS (65757-305-03)
Product NDC 65757-301
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name naltrexone
Dosage Form Name KIT
Route Name
Start Marketing Date 20060613
Marketing Category Name NDA
Labeler Name Alkermes, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of VIVITROL


General Information