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Pregabalin

NDC 71610-619 · Aphena Pharma Solutions - Tennessee, LLC

Generic namePREGABALIN

Dosage formCAPSULE

RouteORAL

Active ingredient(s)PREGABALIN

Strength50 mg/1

DEA scheduleCV

Marketing categoryANDA

Packages

71610-619-53 — 60 CAPSULE in 1 BOTTLE (71610-619-53)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-9699 — PREGABALIN, 71335-9740 — PREGABALIN, 71610-313 — PREGABALIN, 71610-314 — PREGABALIN, 71610-316 — PREGABALIN, 71610-317 — PREGABALIN, 71610-318 — PREGABALIN, 71610-319 — PREGABALIN, 71610-320 — PREGABALIN, 71610-618 — PREGABALIN, 71610-677 — PREGABALIN, 71610-719 — Pregabalin, 71610-754 — PREGABALIN, 71610-758 — Pregabalin, 71610-759 — Pregabalin, 71610-760 — Pregabalin, 71610-765 — PREGABALIN, 71610-792 — Pregabalin, 71610-799 — Pregabalin, 71610-800 — PREGABALIN, +519 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels