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
- 72888-049_49fe33c0-b2ae-e0c1-e063-6294a90a36a4
- Product NDC
- 72888-049
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Pregabalin
- Labeler
- Advagen Pharma Ltd.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220322
- Source listing expiry
- 20271231
Source-listed ingredients
- PREGABALIN — 82.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72888-049-30) · 72888-049-30
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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