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LEVETIRACETAM
LEVETIRACETAM - 49349-058-21 - (LEVETIRACETAM)
Drug Information of LEVETIRACETAM
| Product NDC: | 49349-058 |
| 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: | 49349-058 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076919 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101108 |
Package Information of LEVETIRACETAM
| Package NDC: | 49349-058-21 |
| Package Description: | 120 TABLET in 1 CANISTER (49349-058-21) |
NDC Information of LEVETIRACETAM
| NDC Code | 49349-058-21 |
| Proprietary Name | LEVETIRACETAM |
| Package Description | 120 TABLET in 1 CANISTER (49349-058-21) |
| Product NDC | 49349-058 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LEVETIRACETAM |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101108 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK 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] |
