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
- 71610-887_0b556ed7-7827-40f7-b8fe-4bdf13e8f08c
- Product NDC
- 71610-887
- Form
- CAPSULE
- Composition / generic term
- Pregabalin
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190719
- 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 (71610-887-30) · 71610-887-30
- 56 CAPSULE in 1 BOTTLE (71610-887-46) · 71610-887-46
- 60 CAPSULE in 1 BOTTLE (71610-887-53) · 71610-887-53
- 90 CAPSULE in 1 BOTTLE (71610-887-60) · 71610-887-60
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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