55648-741 NDC - RANITIDINE ()

Drug Information

Product NDC: 55648-741

Proprietary Name: RANITIDINE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: WOCKHARDT LIMITED
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/26/2007

Package Information

No. Package Code Package Description Billing Unit
155648-741-0030000 TABLET, COATED in 1 DRUM (55648-741-00)
255648-741-011 BOTTLE in 1 CARTON (55648-741-01) / 10 TABLET, COATED in 1 BOTTLE
355648-741-021 BOTTLE in 1 CARTON (55648-741-02) / 100 TABLET, COATED in 1 BOTTLE
455648-741-0310 BLISTER PACK in 1 CARTON (55648-741-03) / 10 TABLET, COATED in 1 BLISTER PACK
555648-741-051 BOTTLE in 1 CARTON (55648-741-05) / 500 TABLET, COATED in 1 BOTTLE
655648-741-066000 TABLET, COATED in 1 POUCH (55648-741-06)

NDC Record

Field Name Field Value Definition
PRODUCT NDC55648-741The 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 DATE11/26/2007This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEWOCKHARDT LIMITEDName 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