67296-0756 NDC - ENALAPRIL MALEATE ()

Drug Information

Product NDC: 67296-0756

Proprietary Name: ENALAPRIL MALEATE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: RedPharm Drug, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/11/2009

Package Information

No. Package Code Package Description Billing Unit
167296-0756-130 TABLET in 1 BOTTLE (67296-0756-1)
267296-0756-290 TABLET in 1 BLISTER PACK (67296-0756-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC67296-0756The 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 NAMEENALAPRIL MALEATEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/11/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERedPharm Drug, 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