NDC 69367-329 – Pregabalin

Pregabalin 200 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CV

Product NDC69367-329

Product details

Brand name
Pregabalin
Generic name
Pregabalin
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA208677
Marketed since
August 24, 2021
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Pregabalin →

Package NDC codes (1)

Package NDCDescriptionSince
69367-329-0990 CAPSULE in 1 BOTTLE (69367-329-09)Aug 24, 2021

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