Pregabalin

Product NDC
71610-946
11-digit product format
716100946
Labeler code
71610
Product ID
71610-946_3e9cf925-cb3f-22fc-e063-6394a90a61fe
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
225 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
71610-946-307161009463030 CAPSULE in 1 BOTTLE (71610-946-30) 30 capsule2025-09-10NoNoHistorical
71610-946-467161009464656 CAPSULE in 1 BOTTLE (71610-946-46) 56 capsule2025-09-10NoNoHistorical
71610-946-537161009465360 CAPSULE in 1 BOTTLE (71610-946-53) 60 capsule2025-09-10NoNoHistorical
71610-946-547161009465484 CAPSULE in 1 BOTTLE (71610-946-54) 84 capsule2025-09-10NoNoHistorical
71610-946-9271610094692270 CAPSULE in 1 BOTTLE (71610-946-92) 270 capsule2025-09-10NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
PregabalinAphena Pharma Solutions - Tennessee, LLC2025-09-12HUMAN PRESCRIPTION DRUG LABEL1