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
71610-925_3a124115-06a2-688c-e063-6394a90af648
Product NDC
71610-925
Form
CAPSULE
Composition / generic term
Pregabalin
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Marketing category
ANDA
Marketing start / end (source format)
20210824
Source listing expiry
20261231

Source-listed ingredients

  • PREGABALIN — 300 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 CAPSULE in 1 BOTTLE (71610-925-30) · 71610-925-30
  • 56 CAPSULE in 1 BOTTLE (71610-925-46) · 71610-925-46
  • 60 CAPSULE in 1 BOTTLE (71610-925-53) · 71610-925-53
  • 90 CAPSULE in 1 BOTTLE (71610-925-60) · 71610-925-60
  • 180 CAPSULE in 1 BOTTLE (71610-925-80) · 71610-925-80

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.

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