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Multi-Symptom Cold Daytime - 64092-870-24 - (Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl)

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Drug Information of Multi-Symptom Cold Daytime

Product NDC: 64092-870
Proprietary Name: Multi-Symptom Cold Daytime
Non Proprietary Name: Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl
Active Ingredient(s): 325; 10; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Multi-Symptom Cold Daytime

Product NDC: 64092-870
Labeler Name: GREAT LAKES WHOLESALE, MARKETING, & SALES, INC.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20050715

Package Information of Multi-Symptom Cold Daytime

Package NDC: 64092-870-24
Package Description: 1 BLISTER PACK in 1 BOX (64092-870-24) > 24 TABLET in 1 BLISTER PACK

NDC Information of Multi-Symptom Cold Daytime

NDC Code 64092-870-24
Proprietary Name Multi-Symptom Cold Daytime
Package Description 1 BLISTER PACK in 1 BOX (64092-870-24) > 24 TABLET in 1 BLISTER PACK
Product NDC 64092-870
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050715
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name GREAT LAKES WHOLESALE, MARKETING, & SALES, INC.
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 Multi-Symptom Cold Daytime


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