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
67877-457_59a80208-5cc1-476c-a24b-296bc68e1e0d
Product NDC
67877-457
Form
SOLUTION
Composition / generic term
Pregabalin
Labeler
Ascend Laboratories, LLC
Marketing category
ANDA
Marketing start / end (source format)
20190721
Source listing expiry
20261231

Source-listed ingredients

  • PREGABALIN — 20 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 473 mL in 1 BOTTLE (67877-457-47) · 67877-457-47

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →