63304-537 NDC - LISINOPRIL AND HYDROCHLOROTHIAZIDE ()

Drug Information

Product NDC: 63304-537

Proprietary Name: Lisinopril and Hydrochlorothiazide

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Ranbaxy Pharmaceuticals Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/2/2002

Package Information

No. Package Code Package Description Billing Unit
163304-537-01100 TABLET in 1 BOTTLE (63304-537-01)EA
263304-537-05500 TABLET in 1 BOTTLE (63304-537-05)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC63304-537The 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 NAMELisinopril 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 DATE7/2/2002This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERanbaxy Pharmaceuticals Inc.Name 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