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Levetiracetam
Levetiracetam - 0121-4802-10 - (Levetiracetam)
Drug Information of Levetiracetam
| Product NDC: | 0121-4802 |
| Proprietary Name: | Levetiracetam |
| Non Proprietary Name: | Levetiracetam |
| Active Ingredient(s): | 100 mg/mL & nbsp; Levetiracetam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Levetiracetam
| Product NDC: | 0121-4802 |
| Labeler Name: | Pharmaceutical Associates, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079120 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090920 |
Package Information of Levetiracetam
| Package NDC: | 0121-4802-10 |
| Package Description: | 4 TRAY in 1 CASE (0121-4802-10) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE |
NDC Information of Levetiracetam
| NDC Code | 0121-4802-10 |
| Proprietary Name | Levetiracetam |
| Package Description | 4 TRAY in 1 CASE (0121-4802-10) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE |
| Product NDC | 0121-4802 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levetiracetam |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20090920 |
| Marketing Category Name | ANDA |
| Labeler Name | Pharmaceutical Associates, 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] |
