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Non-Drowsy Sinus Daytime - 64092-845-24 - (Acetaminophen and Phenylephrine HCl)

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Drug Information of Non-Drowsy Sinus Daytime

Product NDC: 64092-845
Proprietary Name: Non-Drowsy Sinus Daytime
Non Proprietary Name: Acetaminophen and Phenylephrine HCl
Active Ingredient(s): 325    mg/1 & nbsp;   Acetaminophen and Phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Non-Drowsy Sinus Daytime

Product NDC: 64092-845
Labeler Name: GREAT LAKES WHOLESALE, MARKETING, & SALES, INC.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20050726

Package Information of Non-Drowsy Sinus Daytime

Package NDC: 64092-845-24
Package Description: 1 BLISTER PACK in 1 CARTON (64092-845-24) > 24 TABLET in 1 BLISTER PACK

NDC Information of Non-Drowsy Sinus Daytime

NDC Code 64092-845-24
Proprietary Name Non-Drowsy Sinus Daytime
Package Description 1 BLISTER PACK in 1 CARTON (64092-845-24) > 24 TABLET in 1 BLISTER PACK
Product NDC 64092-845
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen and Phenylephrine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050726
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name GREAT LAKES WHOLESALE, MARKETING, & SALES, INC.
Substance Name ACETAMINOPHEN
Strength Number 325
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Non-Drowsy Sinus Daytime


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