Evoxac is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Cosette Pharmaceuticals, Inc.. The primary component is Cevimeline Hydrochloride.
| Product ID | 0713-0883_e1f9f25e-98d3-e9e5-e053-2995a90ae380 | 
| NDC | 0713-0883 | 
| Product Type | Human Prescription Drug | 
| Proprietary Name | Evoxac | 
| Generic Name | Cevimeline Hydrochloride | 
| Dosage Form | Capsule | 
| Route of Administration | ORAL | 
| Marketing Start Date | 2022-06-15 | 
| Marketing Category | NDA / | 
| Application Number | NDA020989 | 
| Labeler Name | Cosette Pharmaceuticals, Inc. | 
| Substance Name | CEVIMELINE HYDROCHLORIDE | 
| Active Ingredient Strength | 30 mg/1 | 
| Pharm Classes | Cholinergic Muscarinic Agonists [MoA], Cholinergic Receptor Agonist [EPC] | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2023-12-31 | 
| Marketing Start Date | 2022-06-15 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 0713-0883 | Evoxac | cevimeline hydrochloride | 
| 63395-201 | Evoxac | cevimeline hydrochloride | 
| 0054-0334 | Cevimeline Hydrochloride | Cevimeline Hydrochloride | 
| 0713-0937 | cevimeline hydrochloride | cevimeline hydrochloride | 
| 16571-657 | Cevimeline Hydrochloride | Cevimeline Hydrochloride | 
| 40032-999 | cevimeline hydrochloride | cevimeline hydrochloride | 
| 43386-999 | cevimeline hydrochloride | cevimeline hydrochloride | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  EVOXAC  77641881  3736042 Live/Registered | DAIICHI SANKYO COMPANY, LIMITED 2008-12-31 | 
|  EVOXAC  75837264  2579509 Live/Registered | DAIICHI SANKYO COMPANY, LIMITED 1999-11-01 | 
|  EVOXAC  74350561  1980336 Dead/Cancelled | DAIICHI PHARMACEUTICAL CO., LTD. 1993-01-19 |