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IMITREX
IMITREX - 0173-0736-01 - (sumatriptan succinate)
Drug Information of IMITREX
| Product NDC: | 0173-0736 |
| Proprietary Name: | IMITREX |
| Non Proprietary Name: | sumatriptan succinate |
| Active Ingredient(s): | 50 mg/1 & nbsp; sumatriptan succinate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of IMITREX
| Product NDC: | 0173-0736 |
| Labeler Name: | GlaxoSmithKline LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020132 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20031217 |
Package Information of IMITREX
| Package NDC: | 0173-0736-01 |
| Package Description: | 9 TABLET, FILM COATED in 1 BLISTER PACK (0173-0736-01) |
NDC Information of IMITREX
| NDC Code | 0173-0736-01 |
| Proprietary Name | IMITREX |
| Package Description | 9 TABLET, FILM COATED in 1 BLISTER PACK (0173-0736-01) |
| Product NDC | 0173-0736 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sumatriptan succinate |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20031217 |
| Marketing Category Name | NDA |
| Labeler Name | GlaxoSmithKline LLC |
| Substance Name | SUMATRIPTAN SUCCINATE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
