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Sabril
Sabril - 67386-211-65 - (vigabatrin)
Drug Information of Sabril
| Product NDC: | 67386-211 |
| Proprietary Name: | Sabril |
| Non Proprietary Name: | vigabatrin |
| Active Ingredient(s): | 50 mg/mL & nbsp; vigabatrin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sabril
| Product NDC: | 67386-211 |
| Labeler Name: | Lundbeck LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022006 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090821 |
Package Information of Sabril
| Package NDC: | 67386-211-65 |
| Package Description: | 50 PACKET in 1 CARTON (67386-211-65) > 10 mL in 1 PACKET |
NDC Information of Sabril
| NDC Code | 67386-211-65 |
| Proprietary Name | Sabril |
| Package Description | 50 PACKET in 1 CARTON (67386-211-65) > 10 mL in 1 PACKET |
| Product NDC | 67386-211 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | vigabatrin |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20090821 |
| Marketing Category Name | NDA |
| Labeler Name | Lundbeck LLC |
| Substance Name | VIGABATRIN |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC] |
