Topiramate

Product NDC
80425-0208
11-digit product format
804250208
Labeler code
80425
Product ID
80425-0208_2a99c0c8-93bb-9e14-e063-6394a90a332b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Topiramate
Dosage form
TABLET
Route
ORAL
Labeler
Advanced Rx Pharmacy of Tennessee, LLC
Application
ANDA076343
Marketing category
ANDA
Marketing start
2014-06-14
Substance
TOPIRAMATE
Active strength
25 mg/1
Pharmacologic classes
Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 3A4 Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
0H73WJJ391TOPIRAMATE97240-79-4TOPIRAMATE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
80425-0208-18042502080160 TABLET in 1 BOTTLE (80425-0208-1) 60 tablet2024-02-25NoNoHistorical
80425-0208-28042502080230 TABLET in 1 BOTTLE (80425-0208-2) 30 tablet2023-03-31NoNoHistorical
80425-0208-38042502080390 TABLET in 1 BOTTLE (80425-0208-3) 90 tablet2023-03-31NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Topiramate TabletsAdvanced Rx Pharmacy of Tennessee, LLC2024-12-31HUMAN PRESCRIPTION DRUG LABEL3