Pregabalin

Product NDC
71610-894
11-digit product format
716100894
Labeler code
71610
Product ID
71610-894_3e5239f2-bbf3-18b7-e063-6394a90a895b
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
100 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
71610-894-307161008943030 CAPSULE in 1 BOTTLE (71610-894-30) 30 capsule2025-03-31NoNoHistorical
71610-894-467161008944656 CAPSULE in 1 BOTTLE (71610-894-46) 56 capsule2025-03-31NoNoHistorical
71610-894-537161008945360 CAPSULE in 1 BOTTLE (71610-894-53) 60 capsule2025-03-31NoNoHistorical
71610-894-607161008946090 CAPSULE in 1 BOTTLE (71610-894-60) 90 capsule2025-03-31NoNoHistorical
71610-894-9271610089492270 CAPSULE in 1 BOTTLE (71610-894-92) 270 capsule2025-09-05NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
PregabalinAphena Pharma Solutions - Tennessee, LLC2025-09-08HUMAN PRESCRIPTION DRUG LABEL2