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Alka-Seltzer HEARTBURN - 0280-4085-36 - (Anhydrous Citric Acid and Sodium Bicarbonate)

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Drug Information of Alka-Seltzer HEARTBURN

Product NDC: 0280-4085
Proprietary Name: Alka-Seltzer HEARTBURN
Non Proprietary Name: Anhydrous Citric Acid and Sodium Bicarbonate
Active Ingredient(s): 1000; 1940    mg/1; mg/1 & nbsp;   Anhydrous Citric Acid and Sodium Bicarbonate
Administration Route(s): ORAL
Dosage Form(s): GRANULE, EFFERVESCENT
Coding System: National Drug Codes(NDC)

Labeler Information of Alka-Seltzer HEARTBURN

Product NDC: 0280-4085
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 HEARTBURN

Package NDC: 0280-4085-36
Package Description: 36 PACKET in 1 CARTON (0280-4085-36) > 1 GRANULE, EFFERVESCENT in 1 PACKET

NDC Information of Alka-Seltzer HEARTBURN

NDC Code 0280-4085-36
Proprietary Name Alka-Seltzer HEARTBURN
Package Description 36 PACKET in 1 CARTON (0280-4085-36) > 1 GRANULE, EFFERVESCENT in 1 PACKET
Product NDC 0280-4085
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Anhydrous Citric Acid and Sodium Bicarbonate
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; SODIUM BICARBONATE
Strength Number 1000; 1940
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Alka-Seltzer HEARTBURN


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