57297-766 NDC - AMLODIPINE AND VALSARTAN ()

Drug Information

Product NDC: 57297-766

Proprietary Name: Amlodipine and Valsartan

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:3/30/2015

Package Information

No. Package Code Package Description Billing Unit
157297-766-02500 TABLET in 1 BOTTLE (57297-766-02)
257297-766-0630 TABLET in 1 BOTTLE (57297-766-06)
357297-766-0990 TABLET in 1 BOTTLE (57297-766-09)
457297-766-1110 TABLET in 1 BLISTER PACK (57297-766-11)

NDC Record

Field Name Field Value Definition
PRODUCT NDC57297-766The 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 NAMEAmlodipine and ValsartanThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/30/2015This 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