69202-780 NDC - ULESFIA ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	69202-780-08	1 BOTTLE, PLASTIC in 1 CARTON (69202-780-08) / 227 g in 1 BOTTLE, PLASTIC
2	69202-780-88	2 BOTTLE, PLASTIC in 1 CARTON (69202-780-88) / 227 g in 1 BOTTLE, PLASTIC	GM

Field Name	Field Value	Definition
PRODUCT NDC	69202-780	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	Ulesfia	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	8/17/2015	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.
END MARKETING DATE	3/31/2020	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.
MARKETING CATEGORY NAME	NDA	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
APPLICATION NUMBER	NDA022129	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
LABELER NAME	Lachlan Pharmaceuticals	The translation of the dosage form Code submitted by the firm.