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
- 71610-999_51163e0c-e671-3dc4-e063-6294a90abde9
- Product NDC
- 71610-999
- 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 — 75 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BOTTLE (71610-999-30) · 71610-999-30
- 56 CAPSULE in 1 BOTTLE (71610-999-46) · 71610-999-46
- 60 CAPSULE in 1 BOTTLE (71610-999-53) · 71610-999-53
- 120 CAPSULE in 1 BOTTLE (71610-999-70) · 71610-999-70
- 150 CAPSULE in 1 BOTTLE (71610-999-75) · 71610-999-75
- 180 CAPSULE in 1 BOTTLE (71610-999-80) · 71610-999-80
Source and coverage
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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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