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 | 42043-131_5158c3c8-3c1b-407c-b2d3-3b04736a58b7 |
NDC | 42043-131 |
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 | 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 | 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 |
Billing Unit | EA |
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 | 2.5 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 |