Zonisamide
- Product NDC
- 71205-727
- 11-digit product format
- 712050727
- Labeler code
- 71205
- Product ID
- 71205-727_b4b0ee6a-d4cf-4f29-b9ff-fd5ffc1ce7e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zonisamide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA214492
- Marketing category
- ANDA
- Marketing start
- 2021-07-09
- Substance
- ZONISAMIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC], Carbonic Anhydrase Inhibitors [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE], P-Glycoprotein Inhibitors [MoA], Sulfonamides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 459384H98V | ZONISAMIDE | 68291-97-4 | ZONISAMIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-727-30 | 71205072730 | 30 CAPSULE in 1 BOTTLE (71205-727-30) | 30 capsule | 2022-12-08 | No | No | Historical |
| 71205-727-60 | 71205072760 | 60 CAPSULE in 1 BOTTLE (71205-727-60) | 60 capsule | 2022-12-08 | No | No | Historical |
| 71205-727-90 | 71205072790 | 90 CAPSULE in 1 BOTTLE (71205-727-90) | 90 capsule | 2022-12-08 | No | No | Historical |