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Pregabalin Extended Release

NDC 50228-462 · ScieGen Pharmaceuticals, INC.

Generic namePREGABALIN
Dosage formTABLET, FILM COATED, EXTENDED RELEASE
RouteORAL
Active ingredient(s)PREGABALIN
Strength82.5 mg/1
DEA scheduleCV
Marketing categoryANDA

Packages

50228-462-05 — 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50228-462-05)

50228-462-30 — 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50228-462-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-6793 — PREGABALIN, 50090-7983 — Pregabalin, 50228-350 — PREGABALIN, 50228-351 — PREGABALIN, 50228-352 — PREGABALIN, 50228-353 — PREGABALIN, 50228-354 — PREGABALIN, 50228-355 — PREGABALIN, 50228-356 — PREGABALIN, 50228-357 — 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, 50228-651 — PREGABALIN, 50228-652 — 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.