69729-222 NDC - ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HCL ()

Drug Information

Product NDC: 69729-222

Proprietary Name: Acetaminophen, Chlorpheniramine Maleate, Phenylephrine HCl

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: OPMX LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/26/2019

Package Information

No. Package Code Package Description Billing Unit
169729-222-272 TABLET in 1 POUCH (69729-222-27)
269729-222-3712 TABLET in 1 POUCH (69729-222-37)
369729-222-38144 TABLET in 1 POUCH (69729-222-38)

NDC Record

Field Name Field Value Definition
PRODUCT NDC69729-222The 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, Chlorpheniramine Maleate, Phenylephrine HClThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/26/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEOPMX LLCName 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