NDC 31722-615 – Pregabalin

Pregabalin 200 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CV

Product NDC31722-615

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
31722-615-05500 CAPSULE in 1 BOTTLE (31722-615-05)Oct 8, 2019
31722-615-3110 BLISTER PACK in 1 CARTON (31722-615-31) / 10 CAPSULE in 1 BLISTER PACKOct 8, 2019
31722-615-6060 CAPSULE in 1 BOTTLE (31722-615-60)Oct 8, 2019
31722-615-9090 CAPSULE in 1 BOTTLE (31722-615-90)Oct 8, 2019

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