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Levetiracetam
Levetiracetam - 0093-7795-06 - (Levetiracetam)
Drug Information of Levetiracetam
| Product NDC: | 0093-7795 |
| Proprietary Name: | Levetiracetam |
| Non Proprietary Name: | Levetiracetam |
| Active Ingredient(s): | 500 mg/1 & nbsp; Levetiracetam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Levetiracetam
| Product NDC: | 0093-7795 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091430 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110913 |
Package Information of Levetiracetam
| Package NDC: | 0093-7795-06 |
| Package Description: | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7795-06) |
NDC Information of Levetiracetam
| NDC Code | 0093-7795-06 |
| Proprietary Name | Levetiracetam |
| Package Description | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7795-06) |
| Product NDC | 0093-7795 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levetiracetam |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110913 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | LEVETIRACETAM |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
