58605-303 NDC - MAXI-TUSS CD ()

Drug Information

Product NDC: 58605-303

Proprietary Name: Maxi-Tuss CD

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: MCR American Pharmaceuticals, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/1/2018

Package Information

No. Package Code Package Description Billing Unit
158605-303-1010 mL in 1 BOTTLE, PLASTIC (58605-303-10)
258605-303-16473 mL in 1 BOTTLE, PLASTIC (58605-303-16)ML

NDC Record

Field Name Field Value Definition
PRODUCT NDC58605-303The 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 NAMEMaxi-Tuss CDThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/1/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEMCR American Pharmaceuticals, 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