NDC 58605-303

Maxi-Tuss CD

Chlorpheniramine Maleate, Codeine Phosphate, And Phenylephrine Hydrochloride

Maxi-Tuss CD is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Mcr American Pharmaceuticals, Inc.. The primary component is Chlorpheniramine Maleate; Codeine Phosphate; Phenylephrine Hydrochloride.

Product ID58605-303_41623cf7-6031-4fd8-8e1c-8bb25a08d10f
NDC58605-303
Product TypeHuman Otc Drug
Proprietary NameMaxi-Tuss CD
Generic NameChlorpheniramine Maleate, Codeine Phosphate, And Phenylephrine Hydrochloride
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2018-04-01
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart341
Labeler NameMCR American Pharmaceuticals, Inc.
Substance NameCHLORPHENIRAMINE MALEATE; CODEINE PHOSPHATE; PHENYLEPHRINE HYDROCHLORIDE
Active Ingredient Strength4 mg/5mL; mg/5mL; mg/5mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 58605-303-10

10 mL in 1 BOTTLE, PLASTIC (58605-303-10)
Marketing Start Date2018-04-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58605-303-16 [58605030316]

Maxi-Tuss CD LIQUID
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Billing UnitML
Marketing Start Date2018-04-01

NDC 58605-303-10 [58605030310]

Maxi-Tuss CD LIQUID
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-04-01

Drug Details

Active Ingredients

IngredientStrength
CHLORPHENIRAMINE MALEATE4 mg/5mL

OpenFDA Data

SPL SET ID:e03294a3-1b3e-4d24-ac35-eca00a19db3d
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 2056893

  • © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.