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pregabalin

NDC 43598-295 · Dr.Reddys Laboratories Inc

Generic namepregabalin
Dosage formCAPSULE
RouteORAL
Active ingredient(s)PREGABALIN
Strength150 mg/1
DEA scheduleCV
Marketing categoryANDA

Packages

43598-295-05 — 500 CAPSULE in 1 BOTTLE (43598-295-05)

43598-295-66 — 5 BLISTER PACK in 1 CARTON (43598-295-66) / 10 CAPSULE in 1 BLISTER PACK (43598-295-79)

43598-295-78 — 10 BLISTER PACK in 1 CARTON (43598-295-78) / 10 CAPSULE in 1 BLISTER PACK (43598-295-79)

43598-295-90 — 90 CAPSULE in 1 BOTTLE (43598-295-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43547-508 — pregabalin, 43547-509 — pregabalin, 43547-510 — pregabalin, 43547-511 — pregabalin, 43547-512 — pregabalin, 43547-513 — pregabalin, 43598-291 — pregabalin, 43598-292 — pregabalin, 43598-293 — pregabalin, 43598-294 — pregabalin, 43598-296 — pregabalin, 43598-297 — pregabalin, 43598-298 — pregabalin, 46708-119 — Pregabalin, 46708-120 — Pregabalin, 46708-121 — Pregabalin, 46708-122 — Pregabalin, 46708-123 — Pregabalin, 46708-124 — Pregabalin, 46708-125 — 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.