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Alka-Seltzer Plus - 0280-7055-20 - (Acetaminophen, Dextromethorphan hydrobromide, Chlorpheniramine maleate, and Phenylephrine hydrochloride)

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Drug Information of Alka-Seltzer Plus

Product NDC: 0280-7055
Proprietary Name: Alka-Seltzer Plus
Non Proprietary Name: Acetaminophen, Dextromethorphan hydrobromide, Chlorpheniramine maleate, and Phenylephrine hydrochloride
Active Ingredient(s): 250; 2; 10; 5    mg/1; mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Dextromethorphan hydrobromide, Chlorpheniramine maleate, and Phenylephrine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): GRANULE, EFFERVESCENT
Coding System: National Drug Codes(NDC)

Labeler Information of Alka-Seltzer Plus

Product NDC: 0280-7055
Labeler Name: Bayer HealthCare LLC - Consumer Care
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120702

Package Information of Alka-Seltzer Plus

Package NDC: 0280-7055-20
Package Description: 1 POUCH in 1 CARTON (0280-7055-20) > 20 GRANULE, EFFERVESCENT in 1 POUCH

NDC Information of Alka-Seltzer Plus

NDC Code 0280-7055-20
Proprietary Name Alka-Seltzer Plus
Package Description 1 POUCH in 1 CARTON (0280-7055-20) > 20 GRANULE, EFFERVESCENT in 1 POUCH
Product NDC 0280-7055
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan hydrobromide, Chlorpheniramine maleate, and Phenylephrine hydrochloride
Dosage Form Name GRANULE, EFFERVESCENT
Route Name ORAL
Start Marketing Date 20120702
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Bayer HealthCare LLC - Consumer Care
Substance Name ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 250; 2; 10; 5
Strength Unit mg/1; mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Alka-Seltzer Plus


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