PREGABALIN

Product NDC
72189-241
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
PREGABALIN
Dosage form
CAPSULE
Route
ORAL
Labeler
Direct_Rx
Application
ANDA208677
Marketing category
ANDA
Substance
PREGABALIN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72189-241-3030 CAPSULE in 1 BOTTLE (72189-241-30) 2021-07-23NoHistorical
72189-241-6060 CAPSULE in 1 BOTTLE (72189-241-60) 2021-07-23NoHistorical
72189-241-9090 CAPSULE in 1 BOTTLE (72189-241-90) 2021-07-23NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
PREGABALINDirect_Rx2025-01-17HUMAN PRESCRIPTION DRUG LABEL13