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ROBITUSSIN PEAK COLD DAYTIME COLD PLUS FLU - 0031-8721-20 - (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE)

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Drug Information of ROBITUSSIN PEAK COLD DAYTIME COLD PLUS FLU

Product NDC: 0031-8721
Proprietary Name: ROBITUSSIN PEAK COLD DAYTIME COLD PLUS FLU
Non Proprietary Name: ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE
Active Ingredient(s): 325; 10; 5    mg/1; mg/1; mg/1 & nbsp;   ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of ROBITUSSIN PEAK COLD DAYTIME COLD PLUS FLU

Product NDC: 0031-8721
Labeler Name: Richmond Division of Wyeth
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120415

Package Information of ROBITUSSIN PEAK COLD DAYTIME COLD PLUS FLU

Package NDC: 0031-8721-20
Package Description: 2 BLISTER PACK in 1 CARTON (0031-8721-20) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of ROBITUSSIN PEAK COLD DAYTIME COLD PLUS FLU

NDC Code 0031-8721-20
Proprietary Name ROBITUSSIN PEAK COLD DAYTIME COLD PLUS FLU
Package Description 2 BLISTER PACK in 1 CARTON (0031-8721-20) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 0031-8721
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20120415
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Richmond Division of Wyeth
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 10; 5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of ROBITUSSIN PEAK COLD DAYTIME COLD PLUS FLU


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