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Keppra
Keppra - 21695-070-15 - (levetiracetam)
Drug Information of Keppra
| Product NDC: | 21695-070 |
| Proprietary Name: | Keppra |
| Non Proprietary Name: | levetiracetam |
| Active Ingredient(s): | 500 mg/1 & nbsp; levetiracetam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Keppra
| Product NDC: | 21695-070 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021035 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20000424 |
Package Information of Keppra
| Package NDC: | 21695-070-15 |
| Package Description: | 15 TABLET in 1 DRUM (21695-070-15) |
NDC Information of Keppra
| NDC Code | 21695-070-15 |
| Proprietary Name | Keppra |
| Package Description | 15 TABLET in 1 DRUM (21695-070-15) |
| Product NDC | 21695-070 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | levetiracetam |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20000424 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | LEVETIRACETAM |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
