62756-313 NDC - QUINAPRIL ()

Drug Information

Product NDC: 62756-313

Proprietary Name: Quinapril

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Sun Pharmaceutical Industries Limited
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/18/2009

Package Information

No. Package Code Package Description Billing Unit
162756-313-08100 TABLET, FILM COATED in 1 BOTTLE (62756-313-08)
262756-313-181000 TABLET, FILM COATED in 1 BOTTLE (62756-313-18)
362756-313-8190 TABLET, FILM COATED in 1 BOTTLE (62756-313-81)
462756-313-8330 TABLET, FILM COATED in 1 BOTTLE (62756-313-83)
562756-313-88100 TABLET, FILM COATED in 1 BOTTLE (62756-313-88)

NDC Record

Field Name Field Value Definition
PRODUCT NDC62756-313The 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 NAMEQuinaprilThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/18/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESun Pharmaceutical Industries 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