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Nicardipine hydrochloride

NDC 69238-2691 · Amneal Pharmaceuticals NY LLC

Generic nameNicardipine
Dosage formCAPSULE
RouteORAL
Active ingredient(s)NICARDIPINE HYDROCHLORIDE
Strength20 mg/1
Pharmacologic classCalcium Channel Antagonists [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
Marketing categoryANDA

Packages

69238-2691-1 — 90 CAPSULE in 1 BOTTLE (69238-2691-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55150-183 — NICARDIPINE HYDROCHLORIDE, 62559-205 — Nicardipine Hydrochloride, 62559-206 — Nicardipine Hydrochloride, 65145-197 — Nicardipine Hydrochloride, 65145-198 — Nicardipine Hydrochloride, 65219-818 — Nicardipine Hydrochloride, 67184-0611 — Nicardipine Hydrochloride, 68462-120 — Nicardipine Hydrochloride, 68462-121 — Nicardipine Hydrochloride, 69097-007 — nicardipine hydrochloride, 69238-2692 — Nicardipine, 69292-620 — nicardipine hydrochloride, 69292-621 — nicardipine hydrochloride, 69452-436 — Nicardipine Hydrochloride, 69452-437 — Nicardipine Hydrochloride, 70069-875 — Nicardipine Hydrochloride, 70069-876 — Nicardipine Hydrochloride, 70756-686 — Nicardipine hydrochloride, 71288-204 — nicardipine hydrochloride, 72485-116 — NICARDIPINE HYDROCHLORIDE, +29 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.