NDC 71610-754 – Pregabalin

Pregabalin 200 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CV

Product NDC71610-754

Product details

Brand name
Pregabalin
Generic name
Pregabalin
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA208677
Marketed since
July 19, 2019
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Pregabalin →

Package NDC codes (3)

Package NDCDescriptionSince
71610-754-3030 CAPSULE in 1 BOTTLE (71610-754-30)Nov 28, 2023
71610-754-4656 CAPSULE in 1 BOTTLE (71610-754-46)Nov 28, 2023
71610-754-5360 CAPSULE in 1 BOTTLE (71610-754-53)Nov 28, 2023

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