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LEVETIRACETAM
LEVETIRACETAM - 13811-621-12 - (Levetiracetam)
Drug Information of LEVETIRACETAM
| Product NDC: | 13811-621 |
| 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 |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LEVETIRACETAM
| Product NDC: | 13811-621 |
| Labeler Name: | Trigen Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090906 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120331 |
Package Information of LEVETIRACETAM
| Package NDC: | 13811-621-12 |
| Package Description: | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (13811-621-12) |
NDC Information of LEVETIRACETAM
| NDC Code | 13811-621-12 |
| Proprietary Name | LEVETIRACETAM |
| Package Description | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (13811-621-12) |
| Product NDC | 13811-621 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levetiracetam |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120331 |
| Marketing Category Name | ANDA |
| Labeler Name | Trigen Laboratories, 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] |
