NDC 71610-995 – Pregabalin

Pregabalin 225 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CV

Product NDC71610-995

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
December 10, 2025
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Pregabalin →

Package NDC codes (4)

Package NDCDescriptionSince
71610-995-3030 CAPSULE in 1 BOTTLE (71610-995-30)Mar 20, 2026
71610-995-4656 CAPSULE in 1 BOTTLE (71610-995-46)Mar 25, 2026
71610-995-5360 CAPSULE in 1 BOTTLE (71610-995-53)Mar 20, 2026
71610-995-70120 CAPSULE in 1 BOTTLE (71610-995-70)Mar 20, 2026

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