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Pregabalin

NDC 65862-763 · Aurobindo Pharma Limited

Generic namePregabalin
Dosage formCAPSULE
RouteORAL
Active ingredient(s)PREGABALIN
Strength200 mg/1
DEA scheduleCV
Marketing categoryANDA

Packages

65862-763-05 — 500 CAPSULE in 1 BOTTLE (65862-763-05)

65862-763-78 — 10 BLISTER PACK in 1 CARTON (65862-763-78) / 10 CAPSULE in 1 BLISTER PACK (65862-763-10)

65862-763-90 — 90 CAPSULE in 1 BOTTLE (65862-763-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

64980-413 — PREGABALIN, 64980-414 — PREGABALIN, 64980-415 — PREGABALIN, 64980-416 — PREGABALIN, 64980-417 — PREGABALIN, 65862-758 — Pregabalin, 65862-759 — Pregabalin, 65862-760 — Pregabalin, 65862-761 — Pregabalin, 65862-762 — Pregabalin, 65862-764 — Pregabalin, 65862-765 — Pregabalin, 67046-1494 — Pregabalin, 67046-1628 — Pregabalin, 67046-1680 — Pregabalin, 67877-457 — Pregabalin, 67877-462 — Pregabalin, 67877-463 — Pregabalin, 67877-464 — Pregabalin, 67877-465 — 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.