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levetiracetam
levetiracetam - 50383-241-16 - (levetiracetam)
Drug Information of levetiracetam
| Product NDC: | 50383-241 |
| 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: | 50383-241 |
| Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090601 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120228 |
Package Information of levetiracetam
| Package NDC: | 50383-241-16 |
| Package Description: | 473 mL in 1 BOTTLE (50383-241-16) |
NDC Information of levetiracetam
| NDC Code | 50383-241-16 |
| Proprietary Name | levetiracetam |
| Package Description | 473 mL in 1 BOTTLE (50383-241-16) |
| Product NDC | 50383-241 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | levetiracetam |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20120228 |
| Marketing Category Name | ANDA |
| Labeler Name | Hi-Tech Pharmacal Co., 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] |
