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ZONISAMIDE
ZONISAMIDE - 62756-258-04 - (ZONISAMIDE)
Drug Information of ZONISAMIDE
| Product NDC: | 62756-258 |
| Proprietary Name: | ZONISAMIDE |
| Non Proprietary Name: | ZONISAMIDE |
| Active Ingredient(s): | 25 mg/1 & nbsp; ZONISAMIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZONISAMIDE
| Product NDC: | 62756-258 |
| Labeler Name: | Sun Pharmaceutical Industries Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077634 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060317 |
Package Information of ZONISAMIDE
| Package NDC: | 62756-258-04 |
| Package Description: | 1000 CAPSULE in 1 BOTTLE (62756-258-04) |
NDC Information of ZONISAMIDE
| NDC Code | 62756-258-04 |
| Proprietary Name | ZONISAMIDE |
| Package Description | 1000 CAPSULE in 1 BOTTLE (62756-258-04) |
| Product NDC | 62756-258 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ZONISAMIDE |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20060317 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharmaceutical Industries Limited |
| Substance Name | ZONISAMIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
