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Azelastine Hydrochloride

NDC 70069-091 · Somerset Therapeutics, LLC

Generic nameAzelastine Hydrochloride
Dosage formSOLUTION/ DROPS
RouteOPHTHALMIC
Active ingredient(s)AZELASTINE HYDROCHLORIDE
Strength.5 mg/mL
Pharmacologic classHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

70069-091-01 — 1 BOTTLE in 1 CARTON (70069-091-01) / 6 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

59651-214 — 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, 68788-8514 — AZELASTINE HYDROCHLORIDE, 69168-478 — AZELASTINE HYDROCHLORIDE, 69168-479 — AZELASTINE HYDROCHLORIDE, 69238-2147 — Azelastine, 71205-449 — azelastine hydrochloride, 72162-1388 — azelastine hydrochloride, fluticasone propionate, 72266-141 — Azelastine Hydrochloride, 72603-611 — AZELASTINE HYDROCHLORIDE, 73581-500 — 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.