Zonisamide
- Product NDC
- 0615-1379
- 11-digit product format
- 006151379
- Labeler code
- 0615
- Product ID
- 0615-1379_b15b9eb1-288c-49b6-bc25-520791b5f6fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- zonisamide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA077637
- Marketing category
- ANDA
- Marketing start
- 2012-10-22
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record