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
- 46708-120_b746d2ae-57e4-4a36-9524-35c4aa6b4ef2
- Product NDC
- 46708-120
- Form
- CAPSULE
- Composition / generic term
- Pregabalin
- Labeler
- Alembic Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190719
- Source listing expiry
- 20261231
Source-listed ingredients
- PREGABALIN — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 CARTON (46708-120-10) · 46708-120-10
- 30 CAPSULE in 1 BOTTLE (46708-120-30) · 46708-120-30
- 90 CAPSULE in 1 BOTTLE (46708-120-90) · 46708-120-90
- 1000 CAPSULE in 1 BOTTLE (46708-120-91) · 46708-120-91
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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