68788-9287 NDC - BUTALBITAL, ACETAMINOPHEN, AND CAFFEINE ()

Drug Information

Product NDC: 68788-9287

Proprietary Name: Butalbital, Acetaminophen, and Caffeine

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Preferred Pharmaceuticals Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/8/2015

Package Information

No. Package Code Package Description Billing Unit
168788-9287-1100 TABLET in 1 BOTTLE (68788-9287-1)
268788-9287-220 TABLET in 1 BOTTLE (68788-9287-2)
368788-9287-330 TABLET in 1 BOTTLE (68788-9287-3)
468788-9287-660 TABLET in 1 BOTTLE (68788-9287-6)
568788-9287-8120 TABLET in 1 BOTTLE (68788-9287-8)
668788-9287-990 TABLET in 1 BOTTLE (68788-9287-9)

NDC Record

Field Name Field Value Definition
PRODUCT NDC68788-9287The 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 DATE5/8/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEPreferred Pharmaceuticals Inc.Name 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