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Sudafed PE Pressure plus Pain plus Cough - 50580-550-24 - (Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride)

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Drug Information of Sudafed PE Pressure plus Pain plus Cough

Product NDC: 50580-550
Proprietary Name: Sudafed PE Pressure plus Pain plus Cough
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): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Sudafed PE Pressure plus Pain plus Cough

Product NDC: 50580-550
Labeler Name: McNeil Consumer Healthcare Div. McNeil-PPC, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130225

Package Information of Sudafed PE Pressure plus Pain plus Cough

Package NDC: 50580-550-24
Package Description: 2 BLISTER PACK in 1 CARTON (50580-550-24) > 12 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Sudafed PE Pressure plus Pain plus Cough

NDC Code 50580-550-24
Proprietary Name Sudafed PE Pressure plus Pain plus Cough
Package Description 2 BLISTER PACK in 1 CARTON (50580-550-24) > 12 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 50580-550
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130225
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McNeil Consumer Healthcare Div. McNeil-PPC, 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 Sudafed PE Pressure plus Pain plus Cough


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