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Nicardipine Hydrochloride

NDC 24658-751 · PuraCap Laboratories LLC dba Blu Pharmaceuticals

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

24658-751-90 — 90 CAPSULE in 1 BOTTLE (24658-751-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0143-9542 — Nicardipine Hydrochloride, 0143-9593 — Nicardipine Hydrochloride, 0143-9633 — Nicardipine Hydrochloride, 0143-9634 — Nicardipine Hydrochloride, 0143-9689 — Nicardipine Hydrochloride, 0517-0735 — nicardipine hydrochloride, 24658-750 — Nicardipine Hydrochloride, 25021-333 — Nicardipine Hydrochloride, 35573-457 — nicardipine hydrochloride, 35573-458 — nicardipine hydrochloride, 42571-394 — NICARDIPINE HYDROCHLORIDE, 42806-501 — Nicardipine Hydrochloride, 42806-502 — Nicardipine Hydrochloride, 43066-009 — nicardipine hydrochloride, 43066-016 — nicardipine hydrochloride, 43066-021 — nicardipine hydrochloride, 43066-024 — nicardipine hydrochloride, 43066-026 — nicardipine hydrochloride, 43066-028 — nicardipine hydrochloride, 43066-029 — 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.