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Pregabalin

NDC 70518-3636 · REMEDYREPACK INC.

Generic namePregabalin
Dosage formCAPSULE
RouteORAL
Active ingredient(s)PREGABALIN
Strength50 mg/1
DEA scheduleCV
Marketing categoryANDA

Packages

70518-3636-0 — 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-3636-0)

70518-3636-1 — 60 CAPSULE in 1 BOTTLE, PLASTIC (70518-3636-1)

70518-3636-2 — 120 CAPSULE in 1 BOTTLE, PLASTIC (70518-3636-2)

70518-3636-3 — 30 CAPSULE in 1 BOTTLE, PLASTIC (70518-3636-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69367-429 — Pregabalin, 69367-430 — Pregabalin, 69367-431 — Pregabalin, 70518-2525 — Pregabalin, 70518-2745 — Pregabalin, 70518-2762 — Pregabalin, 70518-2763 — Pregabalin, 70518-3345 — Pregabalin, 70518-3346 — Pregabalin, 70518-3597 — Pregabalin, 70518-3643 — Pregabalin, 70518-3646 — Pregabalin, 70518-3647 — Pregabalin, 70518-3974 — Pregabalin, 70518-4024 — Pregabalin, 70518-4272 — Pregabalin, 70518-4481 — Pregabalin, 70518-4569 — PREGABALIN, 70518-4579 — Pregabalin, 70518-4585 — 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.