0781-2227 NDC - THIOTHIXENE ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	0781-2227-01	100 CAPSULE in 1 BOTTLE (0781-2227-01)	EA
2	0781-2227-10	1000 CAPSULE in 1 BOTTLE (0781-2227-10)
3	0781-2227-13	10 BLISTER PACK in 1 CARTON (0781-2227-13) / 10 CAPSULE in 1 BLISTER PACK

Field Name	Field Value	Definition
PRODUCT NDC	0781-2227	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	Thiothixene	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	6/24/1987	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
END MARKETING DATE	1/31/2016	The translation of the dosage form Code submitted by the firm.
MARKETING CATEGORY NAME	ANDA	The translation of the route code submitted by the firm, indicating route of administration.
APPLICATION NUMBER	ANDA071570	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Sandoz Inc	Name of Company corresponding to the labeler code segment of the Product NDC.