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KEPPRA
KEPPRA - 16590-135-30 - (LEVETIRACETAM)
Drug Information of KEPPRA
| Product NDC: | 16590-135 |
| Proprietary Name: | KEPPRA |
| Non Proprietary Name: | LEVETIRACETAM |
| Active Ingredient(s): | 750 mg/1 & nbsp; LEVETIRACETAM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of KEPPRA
| Product NDC: | 16590-135 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021035 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20000424 |
Package Information of KEPPRA
| Package NDC: | 16590-135-30 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16590-135-30) |
NDC Information of KEPPRA
| NDC Code | 16590-135-30 |
| Proprietary Name | KEPPRA |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16590-135-30) |
| Product NDC | 16590-135 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LEVETIRACETAM |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20000424 |
| Marketing Category Name | NDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | LEVETIRACETAM |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
