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71335-0365 NDC - BUTALBITAL, ACETAMINOPHEN, AND CAFFEINE ()

Drug Information

Product NDC: 71335-0365

Proprietary Name: Butalbital, Acetaminophen, and Caffeine

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:9/13/2012

Package Information

No. Package Code Package Description Billing Unit
171335-0365-084 TABLET in 1 BOTTLE (71335-0365-0)EA
271335-0365-120 TABLET in 1 BOTTLE (71335-0365-1)EA
371335-0365-230 TABLET in 1 BOTTLE (71335-0365-2)EA
471335-0365-360 TABLET in 1 BOTTLE (71335-0365-3)EA
571335-0365-490 TABLET in 1 BOTTLE (71335-0365-4)EA
671335-0365-550 TABLET in 1 BOTTLE (71335-0365-5)EA
771335-0365-66 TABLET in 1 BOTTLE (71335-0365-6)EA
871335-0365-7120 TABLET in 1 BOTTLE (71335-0365-7)EA
971335-0365-840 TABLET in 1 BOTTLE (71335-0365-8)EA
1071335-0365-912 TABLET in 1 BOTTLE (71335-0365-9)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC71335-0365The 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 NAMEButalbital, Acetaminophen, and CaffeineThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/13/2012This 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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