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ROBITUSSIN NIGHT TIME COUGH AND COLD - 0031-8698-13 - (diphenhydramine HCl, phenylephrine HCl)

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Drug Information of ROBITUSSIN NIGHT TIME COUGH AND COLD

Product NDC: 0031-8698
Proprietary Name: ROBITUSSIN NIGHT TIME COUGH AND COLD
Non Proprietary Name: diphenhydramine HCl, phenylephrine HCl
Active Ingredient(s): 6.25; 2.5    mg/5mL; mg/5mL & nbsp;   diphenhydramine HCl, phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of ROBITUSSIN NIGHT TIME COUGH AND COLD

Product NDC: 0031-8698
Labeler Name: Richmond Division of Wyeth
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20060209

Package Information of ROBITUSSIN NIGHT TIME COUGH AND COLD

Package NDC: 0031-8698-13
Package Description: 1 BOTTLE in 1 CARTON (0031-8698-13) > 118 mL in 1 BOTTLE

NDC Information of ROBITUSSIN NIGHT TIME COUGH AND COLD

NDC Code 0031-8698-13
Proprietary Name ROBITUSSIN NIGHT TIME COUGH AND COLD
Package Description 1 BOTTLE in 1 CARTON (0031-8698-13) > 118 mL in 1 BOTTLE
Product NDC 0031-8698
Product Type Name HUMAN OTC DRUG
Non Proprietary Name diphenhydramine HCl, phenylephrine HCl
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20060209
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Richmond Division of Wyeth
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 6.25; 2.5
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of ROBITUSSIN NIGHT TIME COUGH AND COLD


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