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Pregabalin

NDC 71205-396 · Proficient Rx LP

Generic namePREGABALIN
Dosage formCAPSULE
RouteORAL
Active ingredient(s)PREGABALIN
Strength150 mg/1
DEA scheduleCV
Marketing categoryANDA

Packages

71205-396-30 — 30 CAPSULE in 1 BOTTLE (71205-396-30)

71205-396-60 — 60 CAPSULE in 1 BOTTLE (71205-396-60)

71205-396-90 — 90 CAPSULE in 1 BOTTLE (71205-396-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4569 — PREGABALIN, 70518-4579 — Pregabalin, 70518-4585 — Pregabalin, 70518-4654 — Pregabalin, 70518-4715 — Pregabalin, 70518-4716 — Pregabalin, 71205-298 — PREGABALIN, 71205-304 — PREGABALIN, 71205-323 — PREGABALIN, 71205-338 — PREGABALIN, 71205-556 — PREGABALIN, 71205-608 — Pregabalin, 71205-621 — Pregabalin, 71205-639 — Pregabalin, 71205-677 — Pregabalin, 71205-694 — Pregabalin, 71205-696 — Pregabalin, 71205-733 — Pregabalin, 71205-816 — Pregabalin, 71205-869 — 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