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Sabril
Sabril - 67386-111-01 - (vigabatrin)
Drug Information of Sabril
| Product NDC: | 67386-111 |
| Proprietary Name: | Sabril |
| Non Proprietary Name: | vigabatrin |
| Active Ingredient(s): | 500 mg/1 & nbsp; vigabatrin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sabril
| Product NDC: | 67386-111 |
| Labeler Name: | Lundbeck LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020427 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090821 |
Package Information of Sabril
| Package NDC: | 67386-111-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (67386-111-01) |
NDC Information of Sabril
| NDC Code | 67386-111-01 |
| Proprietary Name | Sabril |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (67386-111-01) |
| Product NDC | 67386-111 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | vigabatrin |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20090821 |
| Marketing Category Name | NDA |
| Labeler Name | Lundbeck LLC |
| Substance Name | VIGABATRIN |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC] |
