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