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ROBITUSSIN TO GO COUGH AND CHEST CONGESTION DM - 0031-8712-10 - (dextromethorphan HBr, guaifenesin)

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Drug Information of ROBITUSSIN TO GO COUGH AND CHEST CONGESTION DM

Product NDC: 0031-8712
Proprietary Name: ROBITUSSIN TO GO COUGH AND CHEST CONGESTION DM
Non Proprietary Name: dextromethorphan HBr, guaifenesin
Active Ingredient(s): 2; 20    mg/mL; mg/mL & nbsp;   dextromethorphan HBr, guaifenesin
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of ROBITUSSIN TO GO COUGH AND CHEST CONGESTION DM

Product NDC: 0031-8712
Labeler Name: Richmond Division of Wyeth
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20070731

Package Information of ROBITUSSIN TO GO COUGH AND CHEST CONGESTION DM

Package NDC: 0031-8712-10
Package Description: 10 POUCH in 1 BOX (0031-8712-10) > 10 VIAL, SINGLE-DOSE in 1 POUCH > 10 mL in 1 VIAL, SINGLE-DOSE

NDC Information of ROBITUSSIN TO GO COUGH AND CHEST CONGESTION DM

NDC Code 0031-8712-10
Proprietary Name ROBITUSSIN TO GO COUGH AND CHEST CONGESTION DM
Package Description 10 POUCH in 1 BOX (0031-8712-10) > 10 VIAL, SINGLE-DOSE in 1 POUCH > 10 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0031-8712
Product Type Name HUMAN OTC DRUG
Non Proprietary Name dextromethorphan HBr, guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20070731
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Richmond Division of Wyeth
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 2; 20
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of ROBITUSSIN TO GO COUGH AND CHEST CONGESTION DM


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