Zonisamide
- Product NDC
- 70518-1701
- 11-digit product format
- 705181701
- Labeler code
- 70518
- Product ID
- 70518-1701_c3f30813-082f-6e8a-e053-2995a90a3dea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zonisamide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077634
- Marketing category
- ANDA
- Marketing start
- 2018-11-29
- Marketing end
- 0000-00-00
- Substance
- ZONISAMIDE
- Active strength
- 100 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
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 70518-1701-0 | 70518170100 | 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-1701-0) | 90 capsule | 2018-11-29 | 0000-00-00 | No | No | Current |