Topiramate

Product NDC
50090-6895
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Topiramate
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA076343
Marketing category
ANDA
Substance
TOPIRAMATE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6895-090 TABLET in 1 BOTTLE (50090-6895-0) 2023-12-07NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
TopiramateA-S Medication Solutions2023-12-12HUMAN PRESCRIPTION DRUG LABEL20