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ROBITUSSIN TO GO COUGH AND COLD CF - 0031-8713-10 - (dextromethorphan HBr, guaifenesin, phenylephrine HCl)

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Drug Information of ROBITUSSIN TO GO COUGH AND COLD CF

Product NDC: 0031-8713
Proprietary Name: ROBITUSSIN TO GO COUGH AND COLD CF
Non Proprietary Name: dextromethorphan HBr, guaifenesin, phenylephrine HCl
Active Ingredient(s): 20; 200; 10    mg/10mL; mg/10mL; mg/10mL & nbsp;   dextromethorphan HBr, guaifenesin, phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of ROBITUSSIN TO GO COUGH AND COLD CF

Product NDC: 0031-8713
Labeler Name: Richmond Division of Wyeth
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20080107

Package Information of ROBITUSSIN TO GO COUGH AND COLD CF

Package NDC: 0031-8713-10
Package Description: 10 POUCH in 1 CARTON (0031-8713-10) > 1 VIAL, SINGLE-DOSE in 1 POUCH > 10 mL in 1 VIAL, SINGLE-DOSE

NDC Information of ROBITUSSIN TO GO COUGH AND COLD CF

NDC Code 0031-8713-10
Proprietary Name ROBITUSSIN TO GO COUGH AND COLD CF
Package Description 10 POUCH in 1 CARTON (0031-8713-10) > 1 VIAL, SINGLE-DOSE in 1 POUCH > 10 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0031-8713
Product Type Name HUMAN OTC DRUG
Non Proprietary Name dextromethorphan HBr, guaifenesin, phenylephrine HCl
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20080107
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Richmond Division of Wyeth
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 20; 200; 10
Strength Unit mg/10mL; mg/10mL; mg/10mL
Pharmaceutical Classes

Complete Information of ROBITUSSIN TO GO COUGH AND COLD CF


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