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Naratriptan Hydrochloride
Naratriptan Hydrochloride - 0574-0214-09 - (Naratriptan Hydrochloride)
Drug Information of Naratriptan Hydrochloride
| Product NDC: | 0574-0214 |
| Proprietary Name: | Naratriptan Hydrochloride |
| Non Proprietary Name: | Naratriptan Hydrochloride |
| Active Ingredient(s): | 1.11 mg/1 & nbsp; Naratriptan Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Naratriptan Hydrochloride
| Product NDC: | 0574-0214 |
| Labeler Name: | Paddock Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091326 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100708 |
Package Information of Naratriptan Hydrochloride
| Package NDC: | 0574-0214-09 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (0574-0214-09) > 9 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Naratriptan Hydrochloride
| NDC Code | 0574-0214-09 |
| Proprietary Name | Naratriptan Hydrochloride |
| Package Description | 1 BLISTER PACK in 1 CARTON (0574-0214-09) > 9 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 0574-0214 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Naratriptan Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100708 |
| Marketing Category Name | ANDA |
| Labeler Name | Paddock Laboratories, Inc. |
| Substance Name | NARATRIPTAN HYDROCHLORIDE |
| Strength Number | 1.11 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
