46122-223 NDC - RANITIDINE ()

Drug Information

Product NDC: 46122-223

Proprietary Name: Ranitidine

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Amerisource Bergen
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/6/2013

Package Information

No. Package Code Package Description Billing Unit
146122-223-651 BOTTLE in 1 CARTON (46122-223-65) / 30 TABLET, FILM COATED in 1 BOTTLEEA
246122-223-721 BOTTLE in 1 CARTON (46122-223-72) / 60 TABLET, FILM COATED in 1 BOTTLEEA

NDC Record

Field Name Field Value Definition
PRODUCT NDC46122-223The 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 NAMERanitidineThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/6/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAmerisource BergenName 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