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Nicardipine Hydrochloride

NDC 69452-437 · Bionpharma Inc.

Generic nameNicardipine Hydrochloride
Dosage formCAPSULE
RouteORAL
Active ingredient(s)NICARDIPINE HYDROCHLORIDE
Strength30 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

69452-437-19 — 90 CAPSULE in 1 BOTTLE, PLASTIC (69452-437-19)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65219-818 — Nicardipine Hydrochloride, 67184-0611 — Nicardipine Hydrochloride, 68462-120 — Nicardipine Hydrochloride, 68462-121 — Nicardipine Hydrochloride, 69097-007 — nicardipine hydrochloride, 69238-2691 — Nicardipine, 69238-2692 — Nicardipine, 69292-620 — nicardipine hydrochloride, 69292-621 — nicardipine hydrochloride, 69452-436 — Nicardipine Hydrochloride, 70069-875 — Nicardipine Hydrochloride, 70069-876 — Nicardipine Hydrochloride, 70756-686 — Nicardipine hydrochloride, 71288-204 — nicardipine hydrochloride, 72485-116 — NICARDIPINE HYDROCHLORIDE, 72572-470 — nicardipine hydrochloride, 72819-149 — nicardipine hydrochloride, 82432-103 — Nicardipine Hydrochloride, 87564-027 — nicardipine hydrochloride, 87564-028 — 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.