68084-422 NDC - CHLORPROMAZINE HYDROCHLORIDE ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	68084-422-01	10 BLISTER PACK in 1 CARTON (68084-422-01) / 10 TABLET in 1 BLISTER PACK (68084-422-11)	EA

Field Name	Field Value	Definition
PRODUCT NDC	68084-422	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	Chlorpromazine 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	5/28/2010	This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE	4/30/2014	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	ANDA080439	The translation of the route code submitted by the firm, indicating route of administration.
LABELER NAME	American Health Packaging	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.