76519-1160 NDC - NALTREXONE HYDROCHLORIDE ()

Drug Information

Product NDC: 76519-1160

Proprietary Name: NALTREXONE HYDROCHLORIDE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: H.J. Harkins Company Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/17/2017

Package Information

No. Package Code Package Description Billing Unit
176519-1160-515 TABLET, FILM COATED in 1 CONTAINER (76519-1160-5)

NDC Record

Field Name Field Value Definition
PRODUCT NDC76519-1160The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMENALTREXONE HYDROCHLORIDEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/17/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEH.J. Harkins Company Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 7/26/2021