NDC 71610-759 – Pregabalin

Pregabalin 200 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CV

Product NDC71610-759

Product details

Brand name
Pregabalin
Generic name
Pregabalin
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA209357
Marketed since
July 19, 2019
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Pregabalin →

Package NDC codes (5)

Package NDCDescriptionSince
71610-759-3030 CAPSULE in 1 BOTTLE (71610-759-30)Nov 30, 2023
71610-759-4656 CAPSULE in 1 BOTTLE (71610-759-46)Nov 30, 2023
71610-759-5360 CAPSULE in 1 BOTTLE (71610-759-53)Nov 30, 2023
71610-759-6090 CAPSULE in 1 BOTTLE (71610-759-60)Nov 30, 2023
71610-759-80180 CAPSULE in 1 BOTTLE (71610-759-80)Nov 30, 2023

Other Pregabalin products