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Robitussin Maximum Strength Nighttime Cough DM - 0031-8717-18 - (DEXTROMETHORPHAN HYDROBROMIDE and DOXYLAMINE SUCCINATE)

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Drug Information of Robitussin Maximum Strength Nighttime Cough DM

Product NDC: 0031-8717
Proprietary Name: Robitussin Maximum Strength Nighttime Cough DM
Non Proprietary Name: DEXTROMETHORPHAN HYDROBROMIDE and DOXYLAMINE SUCCINATE
Active Ingredient(s): 30; 12.5    mg/10mL; mg/10mL & nbsp;   DEXTROMETHORPHAN HYDROBROMIDE and DOXYLAMINE SUCCINATE
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Robitussin Maximum Strength Nighttime Cough DM

Product NDC: 0031-8717
Labeler Name: Richmond Division of Wyeth
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130301

Package Information of Robitussin Maximum Strength Nighttime Cough DM

Package NDC: 0031-8717-18
Package Description: 1 BOTTLE in 1 CARTON (0031-8717-18) > 237 mL in 1 BOTTLE

NDC Information of Robitussin Maximum Strength Nighttime Cough DM

NDC Code 0031-8717-18
Proprietary Name Robitussin Maximum Strength Nighttime Cough DM
Package Description 1 BOTTLE in 1 CARTON (0031-8717-18) > 237 mL in 1 BOTTLE
Product NDC 0031-8717
Product Type Name HUMAN OTC DRUG
Non Proprietary Name DEXTROMETHORPHAN HYDROBROMIDE and DOXYLAMINE SUCCINATE
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20130301
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Richmond Division of Wyeth
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE
Strength Number 30; 12.5
Strength Unit mg/10mL; mg/10mL
Pharmaceutical Classes

Complete Information of Robitussin Maximum Strength Nighttime Cough DM


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