0781-5220 NDC - ATENOLOL ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	0781-5220-01	100 TABLET in 1 BOTTLE (0781-5220-01)	EA
2	0781-5220-05	500 TABLET in 1 BOTTLE (0781-5220-05)
3	0781-5220-10	1000 TABLET in 1 BOTTLE (0781-5220-10)	EA

Field Name	Field Value	Definition
PRODUCT NDC	0781-5220	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	Atenolol	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	5/1/1992	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	7/31/2018	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
MARKETING CATEGORY NAME	ANDA	This is the date that the labeler indicates was the start of its marketing of the drug product.
APPLICATION NUMBER	ANDA074052	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.
LABELER NAME	Sandoz Inc	Name of Company corresponding to the labeler code segment of the Product NDC.