Product NDC: | 0603-1384 |
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) |
Product NDC: | 0603-1384 |
Labeler Name: | Qualitest Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090079 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120411 |
Package NDC: | 0603-1384-58 |
Package Description: | 473 mL in 1 BOTTLE (0603-1384-58) |
NDC Code | 0603-1384-58 |
Proprietary Name | Levetiracetam |
Package Description | 473 mL in 1 BOTTLE (0603-1384-58) |
Product NDC | 0603-1384 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Levetiracetam |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20120411 |
Marketing Category Name | ANDA |
Labeler Name | Qualitest Pharmaceuticals |
Substance Name | LEVETIRACETAM |
Strength Number | 100 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |