70518-0925 NDC - VALSARTAN AND HYDROCHLOROTHIAZIDE ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	70518-0925-0	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0925-0)

Field Name	Field Value	Definition
PRODUCT NDC	70518-0925	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	VALSARTAN AND HYDROCHLOROTHIAZIDE	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	12/29/2017	This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE	5/7/2020	This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
MARKETING CATEGORY NAME	ANDA	The translation of the dosage form Code submitted by the firm.
APPLICATION NUMBER	ANDA206083	The translation of the route code submitted by the firm, indicating route of administration.
LABELER NAME	REMEDYREPACK INC.	Name of Company corresponding to the labeler code segment of the Product NDC.