ZONISAMIDE

Product NDC
63629-4565
11-digit product format
636294565
Labeler code
63629
Product ID
63629-4565_ce8e1df2-f8e1-44c4-868f-3dfd7f7b1176
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ZONISAMIDE
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA077634
Marketing category
ANDA
Marketing start
2006-03-17
Marketing end
0000-00-00
Substance
ZONISAMIDE
Active strength
25 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

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
459384H98VZONISAMIDE68291-97-4ZONISAMIDE