57297-102 NDC - VALSARTAN AND HYDROCHLOROTHIAZIDE ()

Drug Information

Product NDC: 57297-102

Proprietary Name: Valsartan and Hydrochlorothiazide

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: LUPIN LIMITED
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/21/2013

Package Information

No. Package Code Package Description Billing Unit
157297-102-02500 TABLET, FILM COATED in 1 BOTTLE (57297-102-02)
257297-102-0990 TABLET, FILM COATED in 1 BOTTLE (57297-102-09)
357297-102-1110 TABLET, FILM COATED in 1 BLISTER PACK (57297-102-11)

NDC Record

Field Name Field Value Definition
PRODUCT NDC57297-102The 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 NAMEValsartan and HydrochlorothiazideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/21/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMELUPIN 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