NDC 71335-1822 – Pregabalin

Pregabalin 200 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CV

Product NDC71335-1822

Product details

Brand name
Pregabalin
Generic name
Pregabalin
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA206912
Marketed since
October 8, 2019
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Pregabalin →

Package NDC codes (3)

Package NDCDescriptionSince
71335-1822-130 CAPSULE in 1 BOTTLE (71335-1822-1)Apr 22, 2021
71335-1822-260 CAPSULE in 1 BOTTLE (71335-1822-2)Apr 13, 2021
71335-1822-390 CAPSULE in 1 BOTTLE (71335-1822-3)Apr 15, 2021

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