United States · FDA National Drug Code directory
Pregabalin
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 71610-994_4ef50a7d-0ef7-25c9-e063-6394a90abbce
- Product NDC
- 71610-994
- Form
- CAPSULE
- Composition / generic term
- PREGABALIN
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251210
- Source listing expiry
- 20271231
Source-listed ingredients
- PREGABALIN — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BOTTLE (71610-994-30) · 71610-994-30
- 56 CAPSULE in 1 BOTTLE (71610-994-46) · 71610-994-46
- 60 CAPSULE in 1 BOTTLE (71610-994-53) · 71610-994-53
- 120 CAPSULE in 1 BOTTLE (71610-994-70) · 71610-994-70
- 270 CAPSULE in 1 BOTTLE (71610-994-92) · 71610-994-92
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →