ZONISAMIDE
- Product NDC
- 63629-4565
- 11-digit product format
- 636294565
- Labeler code
- 63629
- Product ID
- 63629-4565_ce8e1df2-f8e1-44c4-868f-3dfd7f7b1176
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ZONISAMIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077634
- Marketing category
- ANDA
- Marketing start
- 2006-03-17
- Marketing end
- 0000-00-00
- Substance
- ZONISAMIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE],Anti-epileptic Agent [EPC],Sulfonamides [CS],Carbonic Anhydrase Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 459384H98V | ZONISAMIDE | 68291-97-4 | ZONISAMIDE |