Pregabalin

Product NDC
71610-947
11-digit product format
716100947
Labeler code
71610
Product ID
71610-947_3f002caa-e5ca-ea5f-e063-6394a90a470d
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
71610-947-307161009473030 CAPSULE in 1 BOTTLE (71610-947-30) 30 capsule2025-09-16NoNoHistorical
71610-947-537161009475360 CAPSULE in 1 BOTTLE (71610-947-53) 60 capsule2025-09-16NoNoHistorical
71610-947-607161009476090 CAPSULE in 1 BOTTLE (71610-947-60) 90 capsule2025-09-16NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
PregabalinAphena Pharma Solutions - Tennessee, LLC2025-09-17HUMAN PRESCRIPTION DRUG LABEL1