NDC 80425-0399 – Pregabalin

Pregabalin 225 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CV

Product NDC80425-0399

Product details

Brand name
Pregabalin
Generic name
Pregabalin
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA208677
Marketed since
June 4, 2024
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Pregabalin →

Package NDC codes (3)

Package NDCDescriptionSince
80425-0399-130 CAPSULE in 1 BOTTLE (80425-0399-1)Jun 4, 2024
80425-0399-260 CAPSULE in 1 BOTTLE (80425-0399-2)Jun 4, 2024
80425-0399-390 CAPSULE in 1 BOTTLE (80425-0399-3)Jun 4, 2024

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