NDC 72658-0849 – Pregabalin

Pregabalin 200 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CV

Product NDC72658-0849

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 (3)

Package NDCDescriptionSince
72658-0849-160 CAPSULE in 1 BOTTLE (72658-0849-1)Apr 4, 2022
72658-0849-290 CAPSULE in 1 BOTTLE (72658-0849-2)Apr 4, 2022
72658-0849-6500 CAPSULE in 1 BOTTLE (72658-0849-6)Apr 4, 2022

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