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Alka-Seltzer XTRA STRENGTH - 0280-4035-12 - (Anhydrous Citric Acid, Sodium Bicarbonate, and Aspirin)

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Drug Information of Alka-Seltzer XTRA STRENGTH

Product NDC: 0280-4035
Proprietary Name: Alka-Seltzer XTRA STRENGTH
Non Proprietary Name: Anhydrous Citric Acid, Sodium Bicarbonate, and Aspirin
Active Ingredient(s): 1000; 500; 1985    mg/1; mg/1; mg/1 & nbsp;   Anhydrous Citric Acid, Sodium Bicarbonate, and Aspirin
Administration Route(s): ORAL
Dosage Form(s): GRANULE, EFFERVESCENT
Coding System: National Drug Codes(NDC)

Labeler Information of Alka-Seltzer XTRA STRENGTH

Product NDC: 0280-4035
Labeler Name: Bayer HealthCare LLC, Consumer Care
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100302

Package Information of Alka-Seltzer XTRA STRENGTH

Package NDC: 0280-4035-12
Package Description: 12 PACKET in 1 CARTON (0280-4035-12) > 1 GRANULE, EFFERVESCENT in 1 PACKET

NDC Information of Alka-Seltzer XTRA STRENGTH

NDC Code 0280-4035-12
Proprietary Name Alka-Seltzer XTRA STRENGTH
Package Description 12 PACKET in 1 CARTON (0280-4035-12) > 1 GRANULE, EFFERVESCENT in 1 PACKET
Product NDC 0280-4035
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Anhydrous Citric Acid, Sodium Bicarbonate, and Aspirin
Dosage Form Name GRANULE, EFFERVESCENT
Route Name ORAL
Start Marketing Date 20100302
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Bayer HealthCare LLC, Consumer Care
Substance Name ANHYDROUS CITRIC ACID; ASPIRIN; SODIUM BICARBONATE
Strength Number 1000; 500; 1985
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Alka-Seltzer XTRA STRENGTH


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