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Pregabalin

NDC 72205-018 · Novadoz Pharmaceuticals LLC

Generic namePregabalin
Dosage formCAPSULE
RouteORAL
Active ingredient(s)PREGABALIN
Strength300 mg/1
DEA scheduleCV
Marketing categoryANDA

Packages

72205-018-05 — 500 CAPSULE in 1 BOTTLE (72205-018-05)

72205-018-06 — 100 BLISTER PACK in 1 CARTON (72205-018-06) / 10 CAPSULE in 1 BLISTER PACK (72205-018-11)

72205-018-90 — 90 CAPSULE in 1 BOTTLE (72205-018-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72189-251 — PREGABALIN, 72189-269 — PREGABALIN, 72189-328 — pregabalin, 72205-011 — Pregabalin, 72205-012 — Pregabalin, 72205-013 — Pregabalin, 72205-014 — Pregabalin, 72205-015 — Pregabalin, 72205-016 — Pregabalin, 72205-017 — Pregabalin, 72205-077 — PREGABALIN, 72205-078 — PREGABALIN, 72205-079 — PREGABALIN, 72603-352 — Pregabalin, 72603-353 — Pregabalin, 72603-354 — Pregabalin, 72603-355 — Pregabalin, 72603-356 — Pregabalin, 72603-357 — Pregabalin, 72603-358 — 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