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Naratriptan
Naratriptan - 0781-5526-37 - (Naratriptan)
Drug Information of Naratriptan
| Product NDC: | 0781-5526 |
| Proprietary Name: | Naratriptan |
| Non Proprietary Name: | Naratriptan |
| Active Ingredient(s): | 1 mg/1 & nbsp; Naratriptan |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Naratriptan
| Product NDC: | 0781-5526 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090288 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100707 |
Package Information of Naratriptan
| Package NDC: | 0781-5526-37 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (0781-5526-37) > 9 TABLET, COATED in 1 BLISTER PACK |
NDC Information of Naratriptan
| NDC Code | 0781-5526-37 |
| Proprietary Name | Naratriptan |
| Package Description | 1 BLISTER PACK in 1 CARTON (0781-5526-37) > 9 TABLET, COATED in 1 BLISTER PACK |
| Product NDC | 0781-5526 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Naratriptan |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100707 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | NARATRIPTAN HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
