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Tums
Tums - 0135-0522-01 - (calcium carbonate)
Drug Information of Tums
| Product NDC: | 0135-0522 |
| 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, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tums
| Product NDC: | 0135-0522 |
| Labeler Name: | GlaxoSmithKline Consumer Healthcare LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120202 |
Package Information of Tums
| Package NDC: | 0135-0522-01 |
| Package Description: | 2 TABLET, CHEWABLE in 1 POUCH (0135-0522-01) |
NDC Information of Tums
| NDC Code | 0135-0522-01 |
| Proprietary Name | Tums |
| Package Description | 2 TABLET, CHEWABLE in 1 POUCH (0135-0522-01) |
| Product NDC | 0135-0522 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | calcium carbonate |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20120202 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | GlaxoSmithKline Consumer Healthcare LP |
| Substance Name | CALCIUM CARBONATE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
