64725-1782 NDC - NALOXONE HYDROCHLORIDE ()

Drug Information

Product NDC: 64725-1782

Proprietary Name: Naloxone Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: TYA Pharmaceuticals
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/24/1986

Package Information

No. Package Code Package Description Billing Unit
164725-1782-910 mL in 1 BOX (64725-1782-9)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64725-1782The 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 NAMENaloxone 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 DATE9/24/1986This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMETYA PharmaceuticalsName 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