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LEVETIRACETAM
LEVETIRACETAM - 62756-513-40 - (LEVETIRACETAM)
Drug Information of LEVETIRACETAM
| Product NDC: | 62756-513 |
| Proprietary Name: | LEVETIRACETAM |
| Non Proprietary Name: | LEVETIRACETAM |
| Active Ingredient(s): | 100 mg/mL & nbsp; LEVETIRACETAM |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LEVETIRACETAM
| Product NDC: | 62756-513 |
| Labeler Name: | Sun Pharmaceutical Industries Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090754 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100617 |
Package Information of LEVETIRACETAM
| Package NDC: | 62756-513-40 |
| Package Description: | 1 VIAL, SINGLE-USE in 1 CARTON (62756-513-40) > 5 mL in 1 VIAL, SINGLE-USE |
NDC Information of LEVETIRACETAM
| NDC Code | 62756-513-40 |
| Proprietary Name | LEVETIRACETAM |
| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (62756-513-40) > 5 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 62756-513 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LEVETIRACETAM |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20100617 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharmaceutical Industries Limited |
| Substance Name | LEVETIRACETAM |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
