Pregabalin

Product NDC
71610-820
11-digit product format
716100820
Labeler code
71610
Product ID
71610-820_15ea723e-8c08-7ccf-e063-6294a90aaf61
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pregabalin
Dosage form
CAPSULE
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA208677
Marketing category
ANDA
Marketing start
2021-08-24
Substance
PREGABALIN
Active strength
50 mg/1
DEA schedule
CV
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
55JG375S6MPREGABALIN148553-50-8PREGABALIN

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71610-820-307161008203030 CAPSULE in 1 BOTTLE (71610-820-30) 30 capsule2024-04-12NoNoHistorical
71610-820-467161008204656 CAPSULE in 1 BOTTLE (71610-820-46) 56 capsule2024-04-12NoNoHistorical
71610-820-537161008205360 CAPSULE in 1 BOTTLE (71610-820-53) 60 capsule2024-04-12NoNoHistorical
71610-820-607161008206090 CAPSULE in 1 BOTTLE (71610-820-60) 90 capsule2024-04-12NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
PregabalinAphena Pharma Solutions - Tennessee, LLC2024-04-12HUMAN PRESCRIPTION DRUG LABEL1