NDC 0378-0313
Tolmetin Sodium
Tolmetin Sodium
Tolmetin Sodium is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Mylan Pharmaceuticals Inc.. The primary component is Tolmetin Sodium.
Product ID | 0378-0313_71d198cb-78bf-4564-aae5-b7cde7913521 |
NDC | 0378-0313 |
Product Type | Human Prescription Drug |
Proprietary Name | Tolmetin Sodium |
Generic Name | Tolmetin Sodium |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 1994-08-30 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA074473 |
Labeler Name | Mylan Pharmaceuticals Inc. |
Substance Name | TOLMETIN SODIUM |
Active Ingredient Strength | 600 mg/1 |
Pharm Classes | Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |