71335-0920 NDC - ALPRAZOLAM ()

Drug Information

Product NDC: 71335-0920

Proprietary Name: Alprazolam

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Bryant Ranch Prepack
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/25/1998

Package Information

No. Package Code Package Description Billing Unit
171335-0920-130 TABLET in 1 BOTTLE (71335-0920-1)
271335-0920-260 TABLET in 1 BOTTLE (71335-0920-2)
371335-0920-390 TABLET in 1 BOTTLE (71335-0920-3)
471335-0920-4100 TABLET in 1 BOTTLE (71335-0920-4)
571335-0920-510 TABLET in 1 BOTTLE (71335-0920-5)
671335-0920-6120 TABLET in 1 BOTTLE (71335-0920-6)
771335-0920-740 TABLET in 1 BOTTLE (71335-0920-7)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71335-0920The 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 NAMEAlprazolamThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/25/1998This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEBryant Ranch PrepackName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 5/3/2024