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71335-0950 NDC - BUPRENORPHINE ()

Drug Information

Product NDC: 71335-0950

Proprietary Name: BUPRENORPHINE

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:10/25/2017

Package Information

No. Package Code Package Description Billing Unit
171335-0950-160 TABLET in 1 BOTTLE (71335-0950-1)EA
271335-0950-290 TABLET in 1 BOTTLE (71335-0950-2)EA
371335-0950-330 TABLET in 1 BOTTLE (71335-0950-3)EA
471335-0950-47 TABLET in 1 BOTTLE (71335-0950-4)
571335-0950-528 TABLET in 1 BOTTLE (71335-0950-5)
671335-0950-61 TABLET in 1 BOTTLE (71335-0950-6)
771335-0950-712 TABLET in 1 BOTTLE (71335-0950-7)
871335-0950-8120 TABLET in 1 BOTTLE (71335-0950-8)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71335-0950The 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 NAMEBUPRENORPHINEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/25/2017This 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: 4/12/2024
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