Tums - 0135-0482-02 - (famotidine, calcium carbonate and magnesium hydroxide)

Alphabetical Index


Drug Information of Tums

Product NDC: 0135-0482
Proprietary Name: Tums
Non Proprietary Name: famotidine, calcium carbonate and magnesium hydroxide
Active Ingredient(s): 800; 10; 165    mg/1; mg/1; mg/1 & nbsp;   famotidine, calcium carbonate and magnesium hydroxide
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Tums

Product NDC: 0135-0482
Labeler Name: GlaxoSmithKline Consumer Healthcare LP
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077355
Marketing Category: ANDA
Start Marketing Date: 20110608

Package Information of Tums

Package NDC: 0135-0482-02
Package Description: 50 TABLET, CHEWABLE in 1 BOTTLE (0135-0482-02)

NDC Information of Tums

NDC Code 0135-0482-02
Proprietary Name Tums
Package Description 50 TABLET, CHEWABLE in 1 BOTTLE (0135-0482-02)
Product NDC 0135-0482
Product Type Name HUMAN OTC DRUG
Non Proprietary Name famotidine, calcium carbonate and magnesium hydroxide
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20110608
Marketing Category Name ANDA
Labeler Name GlaxoSmithKline Consumer Healthcare LP
Substance Name CALCIUM CARBONATE; FAMOTIDINE; MAGNESIUM HYDROXIDE
Strength Number 800; 10; 165
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Tums


General Information