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AZELASTINE HYDROCHLORIDE

NDC 59651-214 · Aurobindo Pharma Limited

Generic nameAZELASTINE HYDROCHLORIDE
Dosage formSPRAY, METERED
RouteNASAL
Active ingredient(s)AZELASTINE HYDROCHLORIDE
Strength137 ug/1
Pharmacologic classHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

59651-214-30 — 1 BOTTLE, SPRAY in 1 CARTON (59651-214-30) / 200 SPRAY, METERED in 1 BOTTLE, SPRAY

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0480-2157 — Azelastine Hydrochloride and Fluticasone Propionate, 42291-094 — Azelastine, 45802-066 — azelastine hydrochloride, fluticasone propionate, 46708-506 — azelastine hydrochloride, 47335-779 — Azelastine Hydrochloride, 47335-938 — Azelastine Hydrochloride, 50090-2330 — azelastine hydrochloride, 50090-7461 — AZELASTINE HYDROCHLORIDE, 51316-840 — Azelastine Hydrochloride, 58602-020 — AZELASTINE HYDROCHLORIDE, 60505-0578 — AZELASTINE HYDROCHLORIDE, 60505-0833 — azelastine hydrochloride, 60505-0953 — Azelastine hydrochloride and Fluticasone propionate, 61314-308 — azelastine hydrochloride, 62332-506 — Azelastine Hydrochloride Ophthalmic Solution 0.05%, 63629-8612 — azelastine hydrochloride, fluticasone propionate, 65162-676 — Azelastine, 67877-477 — Azelastine, 68083-287 — Azelastine Hydrochloride, 68788-4056 — azelastine hydrochloride, +15 more

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