50436-4856 NDC - BUTALBITAL, ACETAMINOPHEN AND CAFFEINE ()

Drug Information

Product NDC: 50436-4856

Proprietary Name: butalbital, acetaminophen and caffeine

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Unit Dose Services
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/21/1987

Package Information

No. Package Code Package Description Billing Unit
150436-4856-130 TABLET in 1 BOTTLE (50436-4856-1)EA
250436-4856-260 TABLET in 1 BOTTLE (50436-4856-2)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC50436-4856The 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 DATE1/21/1987This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEUnit Dose ServicesName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023