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HORIZANT
HORIZANT - 0173-0806-01 - (gabapentin enacarbil)
Drug Information of HORIZANT
| Product NDC: | 0173-0806 |
| Proprietary Name: | HORIZANT |
| Non Proprietary Name: | gabapentin enacarbil |
| Active Ingredient(s): | 600 mg/1 & nbsp; gabapentin enacarbil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HORIZANT
| Product NDC: | 0173-0806 |
| Labeler Name: | GlaxoSmithKline LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022399 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110407 |
Package Information of HORIZANT
| Package NDC: | 0173-0806-01 |
| Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0173-0806-01) |
NDC Information of HORIZANT
| NDC Code | 0173-0806-01 |
| Proprietary Name | HORIZANT |
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0173-0806-01) |
| Product NDC | 0173-0806 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | gabapentin enacarbil |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110407 |
| Marketing Category Name | NDA |
| Labeler Name | GlaxoSmithKline LLC |
| Substance Name | GABAPENTIN ENACARBIL |
| Strength Number | 600 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
