58805-002 NDC - ACETAMINOPHEN,DEXTROMETHORPHAN,PHENYLEPHRINE ()

Drug Information

Product NDC: 58805-002

Proprietary Name: Acetaminophen,Dextromethorphan,Phenylephrine

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Agile Pharmachem
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/1/2014

Package Information

No. Package Code Package Description Billing Unit
158805-002-088 CARTON in 1 BLISTER PACK (58805-002-08) / 180 CAPSULE, LIQUID FILLED in 1 CARTON
258805-002-147680 CARTON in 1 BLISTER PACK (58805-002-14) / 1 CAPSULE, LIQUID FILLED in 1 CARTON

NDC Record

Field Name Field Value Definition
PRODUCT NDC58805-002The 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,Dextromethorphan,PhenylephrineThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/1/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAgile PharmachemName of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 2/1/2023