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NDC 00135-0074-22 TUMS 750 mg/1 Details
TUMS 750 mg/1
TUMS is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC. The primary component is CALCIUM CARBONATE.
MedlinePlus Drug Summary
Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not enough. Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. It is available with or without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
Related Packages: 00135-0074-22Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Calcium Carbonate
Product Information
| NDC | 00135-0074 |
|---|---|
| Product ID | 0135-0074_2fefb025-c8e3-45d1-a119-042d4099f924 |
| Associated GPIs | 48300010000520 |
| GCN Sequence Number | 002690 |
| GCN Sequence Number Description | calcium carbonate TAB CHEW 300MG(750) ORAL |
| HIC3 | D4B |
| HIC3 Description | ANTACIDS |
| GCN | 07894 |
| HICL Sequence Number | 001163 |
| HICL Sequence Number Description | CALCIUM CARBONATE |
| Brand/Generic | Brand |
| Proprietary Name | TUMS |
| Proprietary Name Suffix | EX |
| Non-Proprietary Name | calcium carbonate |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 750 |
| Active Ingredient Units | mg/1 |
| Substance Name | CALCIUM CARBONATE |
| Labeler Name | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC |
| Pharmaceutical Class | Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA] |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M001 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00135-0074-22 (00135007422)
| NDC Package Code | 0135-0074-22 |
|---|---|
| Billing NDC | 00135007422 |
| Package | 48 TABLET in 1 BOTTLE (0135-0074-22) |
| Marketing Start Date | 2010-01-18 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |