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52959-370 NDC - BUTALBITAL, ASPIRIN AND CAFFEINE ()

Drug Information

Product NDC: 52959-370

Proprietary Name: Butalbital, Aspirin and Caffeine

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: H.J. Harkins Company
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/5/1979

Package Information

No. Package Code Package Description Billing Unit
152959-370-00100 TABLET in 1 BOTTLE, PLASTIC (52959-370-00)EA
252959-370-02120 TABLET in 1 BOTTLE, PLASTIC (52959-370-02)EA
352959-370-1212 TABLET in 1 BOTTLE, PLASTIC (52959-370-12)EA
452959-370-2020 TABLET in 1 BOTTLE, PLASTIC (52959-370-20)EA
552959-370-2525 TABLET in 1 BOTTLE, PLASTIC (52959-370-25)EA
652959-370-3030 TABLET in 1 BOTTLE, PLASTIC (52959-370-30)EA
752959-370-5050 TABLET in 1 BOTTLE, PLASTIC (52959-370-50)EA
852959-370-6060 TABLET in 1 BOTTLE, PLASTIC (52959-370-60)EA
952959-370-9090 TABLET in 1 BOTTLE, PLASTIC (52959-370-90)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC52959-370The 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, Aspirin 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 DATE6/5/1979This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEH.J. Harkins CompanyName 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
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