Zonisamide
- Product NDC
- 71335-0125
- 11-digit product format
- 713350125
- Labeler code
- 71335
- Product ID
- 71335-0125_5f7dacf0-1078-4607-86e8-21db04fecb60
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zonisamide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077651
- Marketing category
- ANDA
- Marketing start
- 2006-01-30
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0125-1 | 71335012501 | 100 CAPSULE in 1 BOTTLE (71335-0125-1) | 100 capsule | 2014-03-10 | 0000-00-00 | No | No | Current |
| 71335-0125-2 | 71335012502 | 90 CAPSULE in 1 BOTTLE (71335-0125-2) | 90 capsule | 2014-03-10 | 0000-00-00 | No | No | Current |
| 71335-0125-3 | 71335012503 | 30 CAPSULE in 1 BOTTLE (71335-0125-3) | 30 capsule | 2014-03-10 | 0000-00-00 | No | No | Current |
| 71335-0125-4 | 71335012504 | 60 CAPSULE in 1 BOTTLE (71335-0125-4) | 60 capsule | 2014-03-10 | 0000-00-00 | No | No | Current |
| 71335-0125-5 | 71335012505 | 120 CAPSULE in 1 BOTTLE (71335-0125-5) | 120 capsule | 2014-03-10 | 0000-00-00 | No | No | Current |