ZoDen DM - 13811-080-30 - (Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride)

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Drug Information of ZoDen DM

Product NDC: 13811-080
Proprietary Name: ZoDen DM
Non Proprietary Name: Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride
Active Ingredient(s): 1; 3; 1.5    mg/mL; mg/mL; mg/mL & nbsp;   Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of ZoDen DM

Product NDC: 13811-080
Labeler Name: TRIGEN Laboratories, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100101

Package Information of ZoDen DM

Package NDC: 13811-080-30
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (13811-080-30) > 30 mL in 1 BOTTLE, DROPPER

NDC Information of ZoDen DM

NDC Code 13811-080-30
Proprietary Name ZoDen DM
Package Description 1 BOTTLE, DROPPER in 1 CARTON (13811-080-30) > 30 mL in 1 BOTTLE, DROPPER
Product NDC 13811-080
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20100101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name TRIGEN Laboratories, Inc.
Substance Name CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 1; 3; 1.5
Strength Unit mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of ZoDen DM


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