Gelusil - 65197-300-20 - (aluminum hydroxide dried gel and magnesium hydroxide and simethicone)

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Drug Information of Gelusil

Product NDC: 65197-300
Proprietary Name: Gelusil
Non Proprietary Name: aluminum hydroxide dried gel and magnesium hydroxide and simethicone
Active Ingredient(s): 200; 24; 200; 1    mg/1; mg/1; mg/1; mg/1 & nbsp;   aluminum hydroxide dried gel and magnesium hydroxide and simethicone
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Gelusil

Product NDC: 65197-300
Labeler Name: WellSpring Pharmaceutical Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part331
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20080924

Package Information of Gelusil

Package NDC: 65197-300-20
Package Description: 2 BLISTER PACK in 1 CARTON (65197-300-20) > 10 TABLET, CHEWABLE in 1 BLISTER PACK

NDC Information of Gelusil

NDC Code 65197-300-20
Proprietary Name Gelusil
Package Description 2 BLISTER PACK in 1 CARTON (65197-300-20) > 10 TABLET, CHEWABLE in 1 BLISTER PACK
Product NDC 65197-300
Product Type Name HUMAN OTC DRUG
Non Proprietary Name aluminum hydroxide dried gel and magnesium hydroxide and simethicone
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20080924
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name WellSpring Pharmaceutical Corporation
Substance Name ALUMINUM HYDROXIDE; DIMETHICONE 410; MAGNESIUM HYDROXIDE; SILICON DIOXIDE
Strength Number 200; 24; 200; 1
Strength Unit mg/1; mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Gelusil


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