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Onfi
Onfi - 67386-311-01 - (clobazam)
Drug Information of Onfi
| Product NDC: | 67386-311 |
| Proprietary Name: | Onfi |
| Non Proprietary Name: | clobazam |
| Active Ingredient(s): | 10 mg/1 & nbsp; clobazam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Onfi
| Product NDC: | 67386-311 |
| Labeler Name: | Lundbeck LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA202067 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20111021 |
Package Information of Onfi
| Package NDC: | 67386-311-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (67386-311-01) > 100 TABLET in 1 BOTTLE |
NDC Information of Onfi
| NDC Code | 67386-311-01 |
| Proprietary Name | Onfi |
| Package Description | 1 BOTTLE in 1 CARTON (67386-311-01) > 100 TABLET in 1 BOTTLE |
| Product NDC | 67386-311 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | clobazam |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111021 |
| Marketing Category Name | NDA |
| Labeler Name | Lundbeck LLC |
| Substance Name | CLOBAZAM |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient],Cytochrome P450 2D6 Inhibitors [MoA] |
