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Severe Sinus Congestion - 59779-574-08 - (Acetaminophen)

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Drug Information of Severe Sinus Congestion

Product NDC: 59779-574
Proprietary Name: Severe Sinus Congestion
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 325; 200; 30    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Severe Sinus Congestion

Product NDC: 59779-574
Labeler Name: WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20080609

Package Information of Severe Sinus Congestion

Package NDC: 59779-574-08
Package Description: 1 BLISTER PACK in 1 CARTON (59779-574-08) > 24 TABLET in 1 BLISTER PACK

NDC Information of Severe Sinus Congestion

NDC Code 59779-574-08
Proprietary Name Severe Sinus Congestion
Package Description 1 BLISTER PACK in 1 CARTON (59779-574-08) > 24 TABLET in 1 BLISTER PACK
Product NDC 59779-574
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080609
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Substance Name ACETAMINOPHEN; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 325; 200; 30
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Severe Sinus Congestion


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