50090-3172 NDC - GLIMEPIRIDE ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	50090-3172-0	30 TABLET in 1 BOTTLE (50090-3172-0)	EA
2	50090-3172-1	100 TABLET in 1 BOTTLE, PLASTIC (50090-3172-1)	EA
3	50090-3172-2	60 TABLET in 1 BOTTLE (50090-3172-2)	EA
4	50090-3172-3	90 TABLET in 1 BOTTLE, PLASTIC (50090-3172-3)	EA
5	50090-3172-4	180 TABLET in 1 BOTTLE, PLASTIC (50090-3172-4)	EA

Field Name	Field Value	Definition
PRODUCT NDC	50090-3172	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	Glimepiride	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	7/14/2015	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	9/30/2024	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	ANDA202112	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	A-S Medication Solutions	Name of Company corresponding to the labeler code segment of the Product NDC.