Product NDC: | 0135-0070 |
Proprietary Name: | TUMS |
Non Proprietary Name: | calcium carbonate |
Active Ingredient(s): | 500 mg/1 & nbsp; calcium carbonate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0135-0070 |
Labeler Name: | GlaxoSmithKline Consumer Heathcare LP |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100310 |
Package NDC: | 0135-0070-48 |
Package Description: | 12 TABLET in 1 PACKAGE (0135-0070-48) |
NDC Code | 0135-0070-48 |
Proprietary Name | TUMS |
Package Description | 12 TABLET in 1 PACKAGE (0135-0070-48) |
Product NDC | 0135-0070 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | calcium carbonate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100310 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | GlaxoSmithKline Consumer Heathcare LP |
Substance Name | CALCIUM CARBONATE |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes |