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ROBITUSSIN COUGH AND CHEST CONGESTION DM MAX - 0031-8668-13 - (dextromethorphan HBr, guaifenesin)

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Drug Information of ROBITUSSIN COUGH AND CHEST CONGESTION DM MAX

Product NDC: 0031-8668
Proprietary Name: ROBITUSSIN COUGH AND CHEST CONGESTION DM MAX
Non Proprietary Name: dextromethorphan HBr, guaifenesin
Active Ingredient(s): 10; 200    mg/5mL; mg/5mL & nbsp;   dextromethorphan HBr, guaifenesin
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of ROBITUSSIN COUGH AND CHEST CONGESTION DM MAX

Product NDC: 0031-8668
Labeler Name: Richmond Division of Wyeth
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20071002

Package Information of ROBITUSSIN COUGH AND CHEST CONGESTION DM MAX

Package NDC: 0031-8668-13
Package Description: 1 BOTTLE in 1 CARTON (0031-8668-13) > 118 mL in 1 BOTTLE

NDC Information of ROBITUSSIN COUGH AND CHEST CONGESTION DM MAX

NDC Code 0031-8668-13
Proprietary Name ROBITUSSIN COUGH AND CHEST CONGESTION DM MAX
Package Description 1 BOTTLE in 1 CARTON (0031-8668-13) > 118 mL in 1 BOTTLE
Product NDC 0031-8668
Product Type Name HUMAN OTC DRUG
Non Proprietary Name dextromethorphan HBr, guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20071002
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Richmond Division of Wyeth
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 200
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of ROBITUSSIN COUGH AND CHEST CONGESTION DM MAX


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