| NDC Code | 0574-0215-09 |
|---|
| Package Description | 9 BLISTER PACK in 1 CARTON (0574-0215-09) > 1 TABLET, FILM COATED in 1 BLISTER PACK |
|---|
| Product NDC | 0574-0215 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Naratriptan Hydrochloride |
|---|
| Non-Proprietary Name | Naratriptan Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20100708 |
|---|
| End Marketing Date | 20180331 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA091326 |
|---|
| Manufacturer | Paddock Laboratories, LLC |
|---|
| Substance Name | NARATRIPTAN HYDROCHLORIDE |
|---|
| Strength | 2.5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
|---|