71335-1907 NDC - ALPRAZOLAM ()

Drug Information

No.	Package Code	Package Description
1	71335-1907-1	30 TABLET in 1 BOTTLE (71335-1907-1)
2	71335-1907-2	60 TABLET in 1 BOTTLE (71335-1907-2)
3	71335-1907-3	90 TABLET in 1 BOTTLE (71335-1907-3)
4	71335-1907-4	28 TABLET in 1 BOTTLE (71335-1907-4)
5	71335-1907-5	120 TABLET in 1 BOTTLE (71335-1907-5)

Field Name	Field Value	Definition
PRODUCT NDC	71335-1907	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	Alprazolam	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	7/9/2018	This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE	10/31/2025	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	ANDA207507	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Bryant Ranch Prepack	Name of Company corresponding to the labeler code segment of the Product NDC.