67296-0329 NDC - DOXYCYCLINE HYCLATE ()

Drug Information

Product NDC: 67296-0329

Proprietary Name: Doxycycline Hyclate

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:7/10/1986

Package Information

No. Package Code Package Description Billing Unit
167296-0329-214 TABLET, FILM COATED in 1 BOTTLE (67296-0329-2)
267296-0329-320 TABLET, FILM COATED in 1 BOTTLE (67296-0329-3)
367296-0329-42 TABLET, FILM COATED in 1 BOTTLE (67296-0329-4)

NDC Record

Field Name Field Value Definition
PRODUCT NDC67296-0329The 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 NAMEDoxycycline HyclateThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/10/1986This 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