Home
>
National Drug Code (NDC)
>
LOTRONEX
LOTRONEX - 65483-895-03 - (alosetron hydrochloride)
Drug Information of LOTRONEX
| Product NDC: | 65483-895 |
| Proprietary Name: | LOTRONEX |
| Non Proprietary Name: | alosetron hydrochloride |
| Active Ingredient(s): | 1 mg/1 & nbsp; alosetron hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LOTRONEX
| Product NDC: | 65483-895 |
| Labeler Name: | Prometheus Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021107 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090209 |
Package Information of LOTRONEX
| Package NDC: | 65483-895-03 |
| Package Description: | 30 TABLET in 1 BOTTLE (65483-895-03) |
NDC Information of LOTRONEX
| NDC Code | 65483-895-03 |
| Proprietary Name | LOTRONEX |
| Package Description | 30 TABLET in 1 BOTTLE (65483-895-03) |
| Product NDC | 65483-895 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | alosetron hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090209 |
| Marketing Category Name | NDA |
| Labeler Name | Prometheus Laboratories Inc. |
| Substance Name | ALOSETRON HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
