Zonisamide
- Product NDC
- 55700-204
- 11-digit product format
- 557000204
- Labeler code
- 55700
- Product ID
- 55700-204_0410c746-773c-4436-a91c-e4debdc1cdd7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- zonisamide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- 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
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record