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Alka-Seltzer Plus - 0280-1435-20 - (Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, and Phenylephrine hydrochloride)

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Drug Information of Alka-Seltzer Plus

Product NDC: 0280-1435
Proprietary Name: Alka-Seltzer Plus
Non Proprietary Name: Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, and Phenylephrine hydrochloride
Active Ingredient(s): 325; 10; 6.25; 5    mg/1; mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, and Phenylephrine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Alka-Seltzer Plus

Product NDC: 0280-1435
Labeler Name: Bayer HealthCare LLC - Consumer Care
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120530

Package Information of Alka-Seltzer Plus

Package NDC: 0280-1435-20
Package Description: 1 BLISTER PACK in 1 CARTON (0280-1435-20) > 20 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Alka-Seltzer Plus

NDC Code 0280-1435-20
Proprietary Name Alka-Seltzer Plus
Package Description 1 BLISTER PACK in 1 CARTON (0280-1435-20) > 20 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 0280-1435
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, and Phenylephrine hydrochloride
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20120530
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Bayer HealthCare LLC - Consumer Care
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 10; 6.25; 5
Strength Unit mg/1; mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Alka-Seltzer Plus


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