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Pregabalin

NDC 69367-429 · Westminster Pharmaceuticals, LLC

Generic namePregabalin
Dosage formCAPSULE
RouteORAL
Active ingredient(s)PREGABALIN
Strength200 mg/1
DEA scheduleCV
Marketing categoryANDA

Packages

69367-429-05 — 500 CAPSULE in 1 BOTTLE (69367-429-05)

69367-429-09 — 90 CAPSULE in 1 BOTTLE (69367-429-09)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69367-327 — Pregabalin, 69367-328 — Pregabalin, 69367-329 — Pregabalin, 69367-330 — Pregabalin, 69367-331 — Pregabalin, 69367-424 — Pregabalin, 69367-425 — Pregabalin, 69367-426 — Pregabalin, 69367-427 — Pregabalin, 69367-428 — Pregabalin, 69367-430 — Pregabalin, 69367-431 — Pregabalin, 70518-2525 — Pregabalin, 70518-2745 — Pregabalin, 70518-2762 — Pregabalin, 70518-2763 — Pregabalin, 70518-3345 — Pregabalin, 70518-3346 — Pregabalin, 70518-3597 — Pregabalin, 70518-3636 — 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