57297-515 NDC - LISINOPRIL ()

Drug Information

Product NDC: 57297-515

Proprietary Name: Lisinopril

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:1/13/2006

Package Information

No. Package Code Package Description Billing Unit
157297-515-01100 TABLET in 1 BOTTLE (57297-515-01)
257297-515-02500 TABLET in 1 BOTTLE (57297-515-02)
357297-515-031000 TABLET in 1 BOTTLE (57297-515-03)
457297-515-055000 TABLET in 1 BOTTLE (57297-515-05)
557297-515-0990 TABLET in 1 BOTTLE (57297-515-09)
657297-515-305000 TABLET in 1 POUCH (57297-515-30)

NDC Record

Field Name Field Value Definition
PRODUCT NDC57297-515The 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 NAMELisinoprilThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/13/2006This 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