NDC 72658-0812 – Pregabalin

Pregabalin 150 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CV

Product NDC72658-0812

Product details

Brand name
Pregabalin
Generic name
Pregabalin
Labeler
Eskayef Pharmaceuticals Limited
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA212988
Marketed since
April 4, 2022
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Pregabalin →

Package NDC codes (5)

Package NDCDescriptionSince
72658-0812-160 CAPSULE in 1 BOTTLE (72658-0812-1)Apr 4, 2022
72658-0812-290 CAPSULE in 1 BOTTLE (72658-0812-2)Apr 4, 2022
72658-0812-36 BLISTER PACK in 1 CARTON (72658-0812-3) / 10 CAPSULE in 1 BLISTER PACKApr 4, 2022
72658-0812-510 BLISTER PACK in 1 CARTON (72658-0812-5) / 10 CAPSULE in 1 BLISTER PACKApr 4, 2022
72658-0812-6500 CAPSULE in 1 BOTTLE (72658-0812-6)Apr 4, 2022

Other Pregabalin products