Levitra (GlaxoSmithKline LLC)
Welcome to the PulseAid listing for the Levitra drug offered from GlaxoSmithKline LLC. This Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | GlaxoSmithKline LLC |
| NON-PROPRIETARY NAME: | vardenafil hydrochloride |
| SUBSTANCE NAME: | VARDENAFIL HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, FILM COATED |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2003-08-25 |
| END MARKETING DATE: | 0000-00-00 |
Levitra HUMAN PRESCRIPTION DRUG Details:
| Item Description | Levitra from GlaxoSmithKline LLC |
| LABELER NAME: | GlaxoSmithKline LLC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 2.5(mg/1) |
| START MARKETING DATE: | 2003-08-25 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0173-0828_4e53cf84-85f4-4597-9f54-29689231fd0e |
| PRODUCT NDC: | 0173-0828 |
| APPLICATION NUMBER: | NDA021400 |
Other VARDENAFIL HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
