Zonisamide

Product NDC
63187-897
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Zonisamide
Dosage form
CAPSULE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA077634
Marketing category
ANDA
Substance
ZONISAMIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
63187-897-3030 CAPSULE in 1 BOTTLE (63187-897-30) 2017-08-01NoHistorical
63187-897-6060 CAPSULE in 1 BOTTLE (63187-897-60) 2017-08-01NoHistorical
63187-897-9090 CAPSULE in 1 BOTTLE (63187-897-90) 2017-08-01NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Zonisamide Capsules, for oral administration Rx onlyProficient Rx LP2022-04-01HUMAN PRESCRIPTION DRUG LABEL5