NDC 31722-616 – Pregabalin

Pregabalin 225 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CV

Product NDC31722-616

Product details

Brand name
Pregabalin
Generic name
Pregabalin
Labeler
Camber Pharmaceuticals, Inc.
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 (4)

Package NDCDescriptionSince
31722-616-05500 CAPSULE in 1 BOTTLE (31722-616-05)Oct 8, 2019
31722-616-3110 BLISTER PACK in 1 CARTON (31722-616-31) / 10 CAPSULE in 1 BLISTER PACKOct 8, 2019
31722-616-6060 CAPSULE in 1 BOTTLE (31722-616-60)Oct 8, 2019
31722-616-9090 CAPSULE in 1 BOTTLE (31722-616-90)Oct 8, 2019

Other Pregabalin products