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Pregabalin

NDC 50228-651 · ScieGen Pharmaceuticals, Inc

Generic namePREGABALIN
Dosage formCAPSULE
RouteORAL
Active ingredient(s)PREGABALIN
Strength225 mg/1
DEA scheduleCV
Marketing categoryANDA

Packages

50228-651-05 — 500 CAPSULE in 1 BOTTLE (50228-651-05)

50228-651-90 — 90 CAPSULE in 1 BOTTLE (50228-651-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50228-357 — PREGABALIN, 50228-462 — PREGABALIN, 50228-463 — PREGABALIN, 50228-464 — PREGABALIN, 50228-645 — PREGABALIN, 50228-646 — PREGABALIN, 50228-647 — PREGABALIN, 50228-648 — PREGABALIN, 50228-649 — PREGABALIN, 50228-650 — PREGABALIN, 50228-652 — PREGABALIN, 50268-497 — Pregabalin, 50268-498 — Pregabalin, 50268-499 — Pregabalin, 50268-500 — Pregabalin, 50268-501 — Pregabalin, 51407-574 — PREGABALIN, 51407-575 — PREGABALIN, 51407-576 — PREGABALIN, 51407-577 — 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.