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Felbatol
Felbatol - 0037-0431-01 - (felbamate)
Drug Information of Felbatol
| Product NDC: | 0037-0431 |
| Proprietary Name: | Felbatol |
| Non Proprietary Name: | felbamate |
| Active Ingredient(s): | 600 mg/1 & nbsp; felbamate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Felbatol
| Product NDC: | 0037-0431 |
| Labeler Name: | Meda Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020189 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19930729 |
Package Information of Felbatol
| Package NDC: | 0037-0431-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (0037-0431-01) |
NDC Information of Felbatol
| NDC Code | 0037-0431-01 |
| Proprietary Name | Felbatol |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0037-0431-01) |
| Product NDC | 0037-0431 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | felbamate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19930729 |
| Marketing Category Name | NDA |
| Labeler Name | Meda Pharmaceuticals Inc. |
| Substance Name | FELBAMATE |
| Strength Number | 600 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
