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Pregabalin

NDC 25000-182 · MARKSANS PHARMA LIMITED

Generic namePregabalin

Dosage formCAPSULE

RouteORAL

Active ingredient(s)PREGABALIN

Strength100 mg/1

DEA scheduleCV

Marketing categoryANDA

Packages

25000-182-07 — 90 CAPSULE in 1 BOTTLE (25000-182-07)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

14445-124 — pregabalin, 14445-125 — pregabalin, 14445-126 — pregabalin, 14445-127 — pregabalin, 14445-128 — pregabalin, 14445-173 — pregabalin, 14445-174 — pregabalin, 25000-179 — Pregabalin, 25000-180 — Pregabalin, 25000-181 — Pregabalin, 25000-183 — Pregabalin, 25000-184 — Pregabalin, 25000-185 — Pregabalin, 25000-186 — Pregabalin, 27808-235 — Pregabalin, 27808-236 — Pregabalin, 27808-237 — Pregabalin, 27808-238 — Pregabalin, 27808-239 — Pregabalin, 27808-240 — 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