| NDC Code | 75834-245-05 | 
|---|
			| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (75834-245-05) | 
|---|
			| Product NDC | 75834-245 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Levetiracetam Extended Release | 
|---|
			
			| Non-Proprietary Name | Levetiracetam | 
|---|
			| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE | 
|---|
			| Usage | ORAL | 
|---|
			| Start Marketing Date | 20200916 | 
|---|
			
			| Marketing Category Name | ANDA | 
|---|
			| Application Number | ANDA201464 | 
|---|
			| Manufacturer | Nivagen Pharmaceuticals, Inc. | 
|---|
			| Substance Name | LEVETIRACETAM | 
|---|
			| Strength | 500 | 
|---|
			| Strength Unit | mg/1 | 
|---|
			| Pharmacy Classes | Decreased Central Nervous System Disorganized Electrical Activity [PE] | 
|---|