64679-972 NDC - FAMOTIDINE ()

Drug Information

Product NDC: 64679-972

Proprietary Name: FAMOTIDINE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Wockhardt USA LLC.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/7/2005

Package Information

No. Package Code Package Description Billing Unit
164679-972-0050000 TABLET in 1 DRUM (64679-972-00)
264679-972-01100 TABLET in 1 BOTTLE (64679-972-01)
364679-972-0210 BLISTER PACK in 1 CARTON (64679-972-02) / 10 TABLET in 1 BLISTER PACK
464679-972-0340000 TABLET in 1 DRUM (64679-972-03)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64679-972The 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 DATE3/7/2005This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEWockhardt USA LLC.Name 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