Pregabalin

Product NDC
71610-871
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pregabalin
Dosage form
CAPSULE
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA205321
Marketing category
ANDA
Substance
PREGABALIN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
71610-871-3030 CAPSULE in 1 BOTTLE (71610-871-30) 2024-12-18NoHistorical
71610-871-4656 CAPSULE in 1 BOTTLE (71610-871-46) 2024-12-18NoHistorical
71610-871-5360 CAPSULE in 1 BOTTLE (71610-871-53) 2024-12-18NoHistorical
71610-871-92270 CAPSULE in 1 BOTTLE (71610-871-92) 2024-12-18NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
PregabalinAphena Pharma Solutions - Tennessee, LLC2024-12-20HUMAN PRESCRIPTION DRUG LABEL1