70518-2949 NDC - DOXEPIN HYDROCHLORIDE ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	70518-2949-0	30 CAPSULE in 1 BLISTER PACK (70518-2949-0)
2	70518-2949-1	100 POUCH in 1 BOX (70518-2949-1) / 1 CAPSULE in 1 POUCH (70518-2949-2)

Field Name	Field Value	Definition
PRODUCT NDC	70518-2949	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	DOXEPIN HYDROCHLORIDE	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
START MARKETING DATE	11/27/2020	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
END MARKETING DATE	1/31/2024	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
MARKETING CATEGORY NAME	ANDA	The translation of the dosage form Code submitted by the firm.
APPLICATION NUMBER	ANDA213063	The translation of the route code submitted by the firm, indicating route of administration.
LABELER NAME	REMEDYREPACK INC.	This is the date that the labeler indicates was the start of its marketing of the drug product.