68151-1021 NDC - QUINAPRIL HYDROCHLORIDE ()

Drug Information

Product NDC: 68151-1021

Proprietary Name: Quinapril Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Carilion Materials Management
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/19/1991

Package Information

No. Package Code Package Description Billing Unit
168151-1021-11 TABLET, FILM COATED in 1 PACKAGE (68151-1021-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC68151-1021The 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 NAMEQuinapril HydrochlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE11/19/1991This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMECarilion Materials ManagementName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 10/4/2019