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Fanatrex
Fanatrex - 43093-105-01 - (Gabapentin)
Drug Information of Fanatrex
| Product NDC: | 43093-105 |
| Proprietary Name: | Fanatrex |
| Non Proprietary Name: | Gabapentin |
| Active Ingredient(s): | & nbsp; Gabapentin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fanatrex
| Product NDC: | 43093-105 |
| Labeler Name: | Fusion Pharmaceuticals LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100515 |
Package Information of Fanatrex
| Package NDC: | 43093-105-01 |
| Package Description: | 1 KIT in 1 KIT (43093-105-01) * 10.5 g in 1 BOTTLE, GLASS * 420 mL in 1 BOTTLE, PLASTIC |
NDC Information of Fanatrex
| NDC Code | 43093-105-01 |
| Proprietary Name | Fanatrex |
| Package Description | 1 KIT in 1 KIT (43093-105-01) * 10.5 g in 1 BOTTLE, GLASS * 420 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 43093-105 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Gabapentin |
| Dosage Form Name | KIT |
| Route Name | ORAL |
| Start Marketing Date | 20100515 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Fusion Pharmaceuticals LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
