| NDC Code | 42658-149-07 |
|---|
| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42658-149-07) |
|---|
| Product NDC | 42658-149 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Levetiracetam |
|---|
| Non-Proprietary Name | Levetiracetam |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20250101 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA207175 |
|---|
| Manufacturer | Hisun Pharmaceuticals USA, Inc. |
|---|
| Substance Name | LEVETIRACETAM |
|---|
| Strength | 750 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Decreased Central Nervous System Disorganized Electrical Activity [PE] |
|---|