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ROBITUSSIN PEAK COLD NIGHTTIME MULTI-SYMPTOM COLD - 0031-8735-18 - (acetaminophen, diphenhydramine HCl, phenylephrine HCl)

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Drug Information of ROBITUSSIN PEAK COLD NIGHTTIME MULTI-SYMPTOM COLD

Product NDC: 0031-8735
Proprietary Name: ROBITUSSIN PEAK COLD NIGHTTIME MULTI-SYMPTOM COLD
Non Proprietary Name: acetaminophen, diphenhydramine HCl, phenylephrine HCl
Active Ingredient(s): 160; 6.25; 2.5    mg/5mL; mg/5mL; mg/5mL & nbsp;   acetaminophen, diphenhydramine HCl, phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of ROBITUSSIN PEAK COLD NIGHTTIME MULTI-SYMPTOM COLD

Product NDC: 0031-8735
Labeler Name: Richmond Division of Wyeth
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110615

Package Information of ROBITUSSIN PEAK COLD NIGHTTIME MULTI-SYMPTOM COLD

Package NDC: 0031-8735-18
Package Description: 1 BOTTLE in 1 CARTON (0031-8735-18) > 237 mL in 1 BOTTLE

NDC Information of ROBITUSSIN PEAK COLD NIGHTTIME MULTI-SYMPTOM COLD

NDC Code 0031-8735-18
Proprietary Name ROBITUSSIN PEAK COLD NIGHTTIME MULTI-SYMPTOM COLD
Package Description 1 BOTTLE in 1 CARTON (0031-8735-18) > 237 mL in 1 BOTTLE
Product NDC 0031-8735
Product Type Name HUMAN OTC DRUG
Non Proprietary Name acetaminophen, diphenhydramine HCl, phenylephrine HCl
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20110615
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Richmond Division of Wyeth
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 160; 6.25; 2.5
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of ROBITUSSIN PEAK COLD NIGHTTIME MULTI-SYMPTOM COLD


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