Naratriptan is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Orchidpharma, Inc. The primary component is Naratriptan Hydrochloride.
| Product ID | 42043-130_5158c3c8-3c1b-407c-b2d3-3b04736a58b7 |
| NDC | 42043-130 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Naratriptan |
| Generic Name | Naratriptan |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2012-12-12 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA091441 |
| Labeler Name | OrchidPharma, Inc |
| Substance Name | NARATRIPTAN HYDROCHLORIDE |
| Active Ingredient Strength | 1 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 | 2020-12-31 |
| Marketing Start Date | 2012-12-12 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA091441 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2012-12-12 |
| Marketing Category | ANDA |
| Application Number | ANDA091441 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-12-12 |
| Ingredient | Strength |
|---|---|
| NARATRIPTAN HYDROCHLORIDE | 1 mg/1 |
| SPL SET ID: | ec5b909e-3406-4154-90aa-19b996e632a8 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0054-0278 | Naratriptan | Naratriptan |
| 0054-0279 | Naratriptan | Naratriptan |
| 0781-5527 | Naratriptan | Naratriptan |
| 23155-054 | naratriptan | naratriptan |
| 23155-055 | naratriptan | naratriptan |
| 42043-130 | Naratriptan | Naratriptan |
| 42043-131 | Naratriptan | Naratriptan |
| 50090-6162 | Naratriptan | Naratriptan |
| 69452-340 | Naratriptan | Naratriptan |
| 69452-341 | Naratriptan | Naratriptan |