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Levetiracetam
Levetiracetam - 0517-3605-25 - (Levetiracetam)
Drug Information of Levetiracetam
| Product NDC: | 0517-3605 |
| Proprietary Name: | Levetiracetam |
| Non Proprietary Name: | Levetiracetam |
| Active Ingredient(s): | 100 mg/mL & nbsp; Levetiracetam |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Levetiracetam
| Product NDC: | 0517-3605 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202143 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120221 |
Package Information of Levetiracetam
| Package NDC: | 0517-3605-25 |
| Package Description: | 25 VIAL, SINGLE-USE in 1 CARTON (0517-3605-25) > 5 mL in 1 VIAL, SINGLE-USE (0517-3605-01) |
NDC Information of Levetiracetam
| NDC Code | 0517-3605-25 |
| Proprietary Name | Levetiracetam |
| Package Description | 25 VIAL, SINGLE-USE in 1 CARTON (0517-3605-25) > 5 mL in 1 VIAL, SINGLE-USE (0517-3605-01) |
| Product NDC | 0517-3605 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levetiracetam |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20120221 |
| Marketing Category Name | ANDA |
| Labeler Name | American Regent, Inc. |
| Substance Name | LEVETIRACETAM |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
