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NDC 16571-0825-09 TOLMETIN SODIUM 600 mg/1 Details
TOLMETIN SODIUM 600 mg/1
TOLMETIN SODIUM is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Rising Pharma Holdings, Inc.. The primary component is TOLMETIN SODIUM.
MedlinePlus Drug Summary
Tolmetin is used to relieve pain, tenderness, swelling, and stiffness caused by osteoarthritis (arthritis caused by a breakdown of the lining of the joints) and rheumatoid arthritis (arthritis caused by swelling of the lining of the joints). Tolmetin is also used to relieve pain, tenderness, swelling, and stiffness caused by juvenile rheumatoid arthritis in children 2 years of age and older. Tolmetin is in a class of medications called NSAIDs. It works by stopping the body's production of a substance that causes pain, fever, and inflammation.
Related Packages: 16571-0825-09Last Updated: 03/24/2024
MedLinePlus Full Drug Details: Tolmetin
Product Information
| NDC | 16571-0825 |
|---|---|
| Product ID | 16571-825_cd0ad97f-9348-4b27-9fd0-a87bc1f93416 |
| Associated GPIs | |
| GCN Sequence Number | 008356 |
| GCN Sequence Number Description | tolmetin sodium TABLET 600 MG ORAL |
| HIC3 | S2B |
| HIC3 Description | NSAIDS, CYCLOOXYGENASE INHIBITOR TYPE ANALGESICS |
| GCN | 35781 |
| HICL Sequence Number | 003725 |
| HICL Sequence Number Description | TOLMETIN SODIUM |
| Brand/Generic | Generic |
| Proprietary Name | TOLMETIN SODIUM |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | tolmetin sodium |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 600 |
| Active Ingredient Units | mg/1 |
| Substance Name | TOLMETIN SODIUM |
| Labeler Name | Rising Pharma Holdings, Inc. |
| Pharmaceutical Class | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA074473 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 16571-0825-09 (16571082509)
| NDC Package Code | 16571-825-09 |
|---|---|
| Billing NDC | 16571082509 |
| Package | 90 TABLET, FILM COATED in 1 BOTTLE (16571-825-09) |
| Marketing Start Date | 2023-04-11 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |