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AMERGE
AMERGE - 0173-0562-00 - (naratriptan hydrochloride)
Drug Information of AMERGE
| Product NDC: | 0173-0562 |
| Proprietary Name: | AMERGE |
| Non Proprietary Name: | naratriptan hydrochloride |
| Active Ingredient(s): | 2.5 mg/1 & nbsp; naratriptan hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AMERGE
| Product NDC: | 0173-0562 |
| Labeler Name: | GlaxoSmithKline LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020763 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19980226 |
Package Information of AMERGE
| Package NDC: | 0173-0562-00 |
| Package Description: | 9 TABLET, FILM COATED in 1 BLISTER PACK (0173-0562-00) |
NDC Information of AMERGE
| NDC Code | 0173-0562-00 |
| Proprietary Name | AMERGE |
| Package Description | 9 TABLET, FILM COATED in 1 BLISTER PACK (0173-0562-00) |
| Product NDC | 0173-0562 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | naratriptan hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19980226 |
| Marketing Category Name | NDA |
| Labeler Name | GlaxoSmithKline LLC |
| Substance Name | NARATRIPTAN HYDROCHLORIDE |
| Strength Number | 2.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
