21695-242 NDC - ACETAMINOPHEN AND CODEINE PHOSPHATE ()

Drug Information

Product NDC: 21695-242

Proprietary Name: ACETAMINOPHEN AND CODEINE PHOSPHATE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Rebel Distributors Corp.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/29/2009

Package Information

No. Package Code Package Description Billing Unit
121695-242-1212 TABLET in 1 BOTTLE (21695-242-12)EA
221695-242-1515 TABLET in 1 BOTTLE (21695-242-15)EA
321695-242-1818 TABLET in 1 BOTTLE (21695-242-18)EA
421695-242-2020 TABLET in 1 BOTTLE (21695-242-20)EA
521695-242-2828 TABLET in 1 BOTTLE (21695-242-28)EA
621695-242-3030 TABLET in 1 BOTTLE (21695-242-30)EA
721695-242-4040 TABLET in 1 BOTTLE (21695-242-40)EA
821695-242-6060 TABLET in 1 BOTTLE (21695-242-60)EA
921695-242-9090 TABLET in 1 BOTTLE (21695-242-90)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC21695-242The 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 DATE6/29/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERebel Distributors Corp.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