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Levetiracetam
Levetiracetam - 51991-649-36 - (Levetiracetam)
Drug Information of Levetiracetam
| Product NDC: | 51991-649 |
| Proprietary Name: | Levetiracetam |
| Non Proprietary Name: | Levetiracetam |
| Active Ingredient(s): | 750 mg/1 & nbsp; Levetiracetam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Levetiracetam
| Product NDC: | 51991-649 |
| Labeler Name: | Breckenridge Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090511 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111101 |
Package Information of Levetiracetam
| Package NDC: | 51991-649-36 |
| Package Description: | 120 TABLET in 1 BOTTLE (51991-649-36) |
NDC Information of Levetiracetam
| NDC Code | 51991-649-36 |
| Proprietary Name | Levetiracetam |
| Package Description | 120 TABLET in 1 BOTTLE (51991-649-36) |
| Product NDC | 51991-649 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levetiracetam |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111101 |
| Marketing Category Name | ANDA |
| Labeler Name | Breckenridge Pharmaceutical, Inc. |
| Substance Name | LEVETIRACETAM |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
