TUMS - 0135-0521-01 - (calcium carbonate)

Alphabetical Index


Drug Information of TUMS

Product NDC: 0135-0521
Proprietary Name: TUMS
Non Proprietary Name: calcium carbonate
Active Ingredient(s): 750    mg/1 & nbsp;   calcium carbonate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of TUMS

Product NDC: 0135-0521
Labeler Name: GlaxoSmithKline Consumer Heathcare LP
Product Type: HUMAN OTC DRUG
FDA Application Number: part331
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110323

Package Information of TUMS

Package NDC: 0135-0521-01
Package Description: 8 TABLET in 1 PACKAGE (0135-0521-01)

NDC Information of TUMS

NDC Code 0135-0521-01
Proprietary Name TUMS
Package Description 8 TABLET in 1 PACKAGE (0135-0521-01)
Product NDC 0135-0521
Product Type Name HUMAN OTC DRUG
Non Proprietary Name calcium carbonate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110323
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name GlaxoSmithKline Consumer Heathcare LP
Substance Name CALCIUM CARBONATE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of TUMS


General Information