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 |