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
- 82804-943_34846423-e747-42c5-9bcd-f99c557c4f67
- Product NDC
- 82804-943
- Form
- CAPSULE
- Composition / generic term
- Pregabalin
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251117
- Source listing expiry
- 20271231
Source-listed ingredients
- PREGABALIN — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (82804-943-00) · 82804-943-00
- 1000 CAPSULE in 1 BOTTLE (82804-943-11) · 82804-943-11
- 30 CAPSULE in 1 BOTTLE (82804-943-30) · 82804-943-30
- 500 CAPSULE in 1 BOTTLE (82804-943-55) · 82804-943-55
- 60 CAPSULE in 1 BOTTLE (82804-943-60) · 82804-943-60
- 270 CAPSULE in 1 BOTTLE (82804-943-67) · 82804-943-67
- 120 CAPSULE in 1 BOTTLE (82804-943-72) · 82804-943-72
- 180 CAPSULE in 1 BOTTLE (82804-943-78) · 82804-943-78
- 90 CAPSULE in 1 BOTTLE (82804-943-90) · 82804-943-90
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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