NDC 72658-0809 – Pregabalin

Pregabalin 50 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CV

Product NDC72658-0809

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
72658-0809-160 CAPSULE in 1 BOTTLE (72658-0809-1)Apr 4, 2022
72658-0809-290 CAPSULE in 1 BOTTLE (72658-0809-2)Apr 4, 2022
72658-0809-36 BLISTER PACK in 1 CARTON (72658-0809-3) / 10 CAPSULE in 1 BLISTER PACKApr 4, 2022
72658-0809-510 BLISTER PACK in 1 CARTON (72658-0809-5) / 10 CAPSULE in 1 BLISTER PACKApr 4, 2022
72658-0809-6500 CAPSULE in 1 BOTTLE (72658-0809-6)Apr 4, 2022

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