0536-1022 NDC - ALL DAY RELIEF ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	0536-1022-01	1 BOTTLE in 1 CARTON (0536-1022-01) / 100 TABLET in 1 BOTTLE	EA
2	0536-1022-06	1 BOTTLE in 1 CARTON (0536-1022-06) / 50 TABLET in 1 BOTTLE	EA

Field Name	Field Value	Definition
PRODUCT NDC	0536-1022	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	All Day Relief	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	3/10/2014	The translation of the dosage form Code submitted by the firm.
END MARKETING DATE	12/31/2018	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	ANDA	This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
APPLICATION NUMBER	ANDA090545	Name of Company corresponding to the labeler code segment of the Product NDC.
LABELER NAME	Rugby Laboratories