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Alka Seltzer - 53666-403-15 - (ASPIRIN, ANHYDROUS CITRIC ACID, SODIUM BICARBONATE)

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Drug Information of Alka Seltzer

Product NDC: 53666-403
Proprietary Name: Alka Seltzer
Non Proprietary Name: ASPIRIN, ANHYDROUS CITRIC ACID, SODIUM BICARBONATE
Active Ingredient(s): 1000; 325; 1916    mg/1; mg/1; mg/1 & nbsp;   ASPIRIN, ANHYDROUS CITRIC ACID, SODIUM BICARBONATE
Administration Route(s): ORAL
Dosage Form(s): TABLET, EFFERVESCENT
Coding System: National Drug Codes(NDC)

Labeler Information of Alka Seltzer

Product NDC: 53666-403
Labeler Name: Salimex, S.A.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121010

Package Information of Alka Seltzer

Package NDC: 53666-403-15
Package Description: 150 BOX in 1 CASE (53666-403-15) > 12 TABLET, EFFERVESCENT in 1 BOX (53666-403-33)

NDC Information of Alka Seltzer

NDC Code 53666-403-15
Proprietary Name Alka Seltzer
Package Description 150 BOX in 1 CASE (53666-403-15) > 12 TABLET, EFFERVESCENT in 1 BOX (53666-403-33)
Product NDC 53666-403
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ASPIRIN, ANHYDROUS CITRIC ACID, SODIUM BICARBONATE
Dosage Form Name TABLET, EFFERVESCENT
Route Name ORAL
Start Marketing Date 20121010
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Salimex, S.A.
Substance Name ANHYDROUS CITRIC ACID; ASPIRIN; SODIUM BICARBONATE
Strength Number 1000; 325; 1916
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Alka Seltzer


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