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Pregabalin

NDC 47335-689 · Sun Pharmaceutical Industries, Inc.

Generic namePregabalin
Dosage formCAPSULE
RouteORAL
Active ingredient(s)PREGABALIN
Strength100 mg/1
DEA scheduleCV
Marketing categoryANDA

Packages

47335-689-08 — 100 CAPSULE in 1 BOTTLE (47335-689-08)

47335-689-18 — 1000 CAPSULE in 1 BOTTLE (47335-689-18)

47335-689-83 — 30 CAPSULE in 1 BOTTLE (47335-689-83)

47335-689-88 — 100 CAPSULE in 1 BOTTLE (47335-689-88)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

46708-120 — Pregabalin, 46708-121 — Pregabalin, 46708-122 — Pregabalin, 46708-123 — Pregabalin, 46708-124 — Pregabalin, 46708-125 — Pregabalin, 46708-126 — Pregabalin, 47335-686 — Pregabalin, 47335-687 — Pregabalin, 47335-688 — Pregabalin, 47335-690 — Pregabalin, 47335-691 — Pregabalin, 47335-692 — Pregabalin, 47335-693 — Pregabalin, 50090-5038 — PREGABALIN, 50090-5071 — Pregabalin, 50090-6503 — Pregabalin, 50090-6504 — Pregabalin, 50090-6793 — PREGABALIN, 50090-7983 — 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.