69025-103 NDC - TENOFOVIR DISOPROXIL FUMARATE ()

Drug Information

Product NDC: 69025-103

Proprietary Name: tenofovir disoproxil fumarate

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	AIZANT DRUG RESEARCH SOLUTIONS PVT LTD
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	1/26/2018

No.	Package Code	Package Description	Billing Unit
1	69025-103-01	30 TABLET, FILM COATED in 1 BOTTLE (69025-103-01)

Field Name	Field Value	Definition
PRODUCT NDC	69025-103	The 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 NAME	tenofovir disoproxil fumarate	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	1/26/2018	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	AIZANT DRUG RESEARCH SOLUTIONS PVT LTD	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