Product NDC: | 31722-537 |
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) |
Product NDC: | 31722-537 |
Labeler Name: | Camber Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090515 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120109 |
Package NDC: | 31722-537-12 |
Package Description: | 12 BOTTLE in 1 CASE (31722-537-12) > 120 TABLET, FILM COATED in 1 BOTTLE |
NDC Code | 31722-537-12 |
Proprietary Name | Levetiracetam |
Package Description | 12 BOTTLE in 1 CASE (31722-537-12) > 120 TABLET, FILM COATED in 1 BOTTLE |
Product NDC | 31722-537 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Levetiracetam |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20120109 |
Marketing Category Name | ANDA |
Labeler Name | Camber Pharmaceuticals |
Substance Name | LEVETIRACETAM |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |