NDC 69452-341
Naratriptan
Naratriptan
Naratriptan is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Bionpharma Inc.. The primary component is Naratriptan Hydrochloride.
| Product ID | 69452-341_81b216d9-f05f-473c-97f6-e3b7ffc63be6 |
| NDC | 69452-341 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Naratriptan |
| Generic Name | Naratriptan |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2022-04-11 |
| Marketing Category | ANDA / |
| Application Number | ANDA091441 |
| Labeler Name | Bionpharma Inc. |
| Substance Name | NARATRIPTAN HYDROCHLORIDE |
| Active Ingredient Strength | 3 mg/1 |
| Pharm Classes | Serotonin 1b Receptor Agonists [MoA], Serotonin 1d Receptor Agonists [MoA], Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |