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
- 71335-2339_7c52e39f-79ad-4ffa-95df-f66fc4c48113
- Product NDC
- 71335-2339
- Form
- CAPSULE
- Composition / generic term
- PREGABALIN
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190719
- 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 (71335-2339-1) · 71335-2339-1
- 60 CAPSULE in 1 BOTTLE (71335-2339-2) · 71335-2339-2
- 90 CAPSULE in 1 BOTTLE (71335-2339-3) · 71335-2339-3
- 120 CAPSULE in 1 BOTTLE (71335-2339-4) · 71335-2339-4
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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