NDC 65757-301

VIVITROL

Naltrexone

VIVITROL is a Kit in the Human Prescription Drug category. It is labeled and distributed by Alkermes, Inc.. The primary component is .

• Product ID: 65757-301_7e88c2c9-c3a9-4d25-b780-2b8aa1c66a00
• NDC: 65757-301
• Product Type: Human Prescription Drug
• Proprietary Name: VIVITROL
• Generic Name: Naltrexone
• Dosage Form: Kit
• Marketing Start Date: 2006-06-13
• Marketing Category: NDA /
• Application Number: NDA021897
• Labeler Name: Alkermes, Inc.
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 65757-301-01

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)

• Marketing Start Date: 2006-06-13
• NDC Exclude Flag: N
• Sample Package?: Y

NDC SPL Data Element Entries

NDC 65757-301-01 [65757030101]

VIVITROL KIT

• Marketing Category: NDA
• Application Number: NDA021897
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2006-06-13
• Marketing End Date: 2015-12-08

Drug Details

NDC Crossover Matching brand name "VIVITROL" or generic name "Naltrexone"

NDC	Brand Name	Generic Name
65757-300	VIVITROL	naltrexone
65757-301	VIVITROL	naltrexone
69364-3143	Naltrexone	naltrexone