0121-1008 NDC - ACETAMINOPHEN AND CODEINE PHOSPHATE ()

Drug Information

Product NDC: 0121-1008

Proprietary Name: Acetaminophen and Codeine Phosphate

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Pharmaceutical Associates, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/21/1981

Package Information

No. Package Code Package Description Billing Unit
10121-1008-0010 TRAY in 1 CASE (0121-1008-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 12.5 mL in 1 CUP, UNIT-DOSE (0121-1008-12)ML

NDC Record

Field Name Field Value Definition
PRODUCT NDC0121-1008The 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 NAMEAcetaminophen and Codeine PhosphateThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/21/1981This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEPharmaceutical Associates, 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