NDC 69367-430 – Pregabalin

Pregabalin 225 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CV

Product NDC69367-430

Product details

Brand name
Pregabalin
Generic name
Pregabalin
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA212988
Marketed since
November 17, 2025
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Pregabalin →

Package NDC codes (2)

Package NDCDescriptionSince
69367-430-05500 CAPSULE in 1 BOTTLE (69367-430-05)Nov 17, 2025
69367-430-0990 CAPSULE in 1 BOTTLE (69367-430-09)Nov 17, 2025

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