61715-064 NDC - FAMOTIDINE ()

Drug Information

Product NDC: 61715-064

Proprietary Name: Famotidine

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Kinray
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/15/2012

Package Information

No. Package Code Package Description Billing Unit
161715-064-251 BOTTLE in 1 CARTON (61715-064-25) / 25 TABLET, FILM COATED in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC61715-064The 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 NAMEFamotidineThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/15/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEKinrayName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023