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Pregabalin

NDC 65862-758 · Aurobindo Pharma Limited

Generic namePregabalin
Dosage formCAPSULE
RouteORAL
Active ingredient(s)PREGABALIN
Strength25 mg/1
DEA scheduleCV
Marketing categoryANDA

Packages

65862-758-05 — 500 CAPSULE in 1 BOTTLE (65862-758-05)

65862-758-78 — 10 BLISTER PACK in 1 CARTON (65862-758-78) / 10 CAPSULE in 1 BLISTER PACK (65862-758-10)

65862-758-90 — 90 CAPSULE in 1 BOTTLE (65862-758-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63629-8239 — PREGABALIN, 63629-8248 — PREGABALIN, 64980-410 — PREGABALIN, 64980-411 — PREGABALIN, 64980-412 — PREGABALIN, 64980-413 — PREGABALIN, 64980-414 — PREGABALIN, 64980-415 — PREGABALIN, 64980-416 — PREGABALIN, 64980-417 — PREGABALIN, 65862-759 — Pregabalin, 65862-760 — Pregabalin, 65862-761 — Pregabalin, 65862-762 — Pregabalin, 65862-763 — Pregabalin, 65862-764 — Pregabalin, 65862-765 — Pregabalin, 67046-1494 — Pregabalin, 67046-1628 — Pregabalin, 67046-1680 — 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.