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Fexofenadine HCL

NDC 73581-009 · YYBA Corp

Generic nameFexofenadine HCL
Dosage formTABLET
RouteORAL
Active ingredient(s)FEXOFENADINE HYDROCHLORIDE
Strength180 mg/1
Pharmacologic classHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

73581-009-01 — 10 TABLET in 1 BOTTLE (73581-009-01)

73581-009-04 — 40 TABLET in 1 BOTTLE (73581-009-04)

73581-009-10 — 100 TABLET in 1 BOTTLE (73581-009-10)

73581-009-20 — 200 TABLET in 1 BOTTLE (73581-009-20)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72090-058 — FEXOFENADINE HYDROCHLORIDE, 72090-068 — Fexofenadine Hydrochloride, 72288-537 — fexofenadine hydrochloride, 72288-722 — Fexofenadine Hydrochloride, 72288-847 — fexofenadine hydrochloride, 72476-192 — Fexofenadine Hydrochloride, 72476-847 — fexofenadine hydrochloride, 72559-027 — Fexofenadine Hydrochloride 180 mg, 72559-028 — Fexofenadine Hydrochloride 180 mg, 72789-196 — Fexofenadine HCL, 73581-010 — Fexofenadine HCL, 73581-011 — FEXOFENADINE HYDROCHLORIDE, 73581-012 — Fexofenadine, 73581-025 — Fexofenadine Hydrochloride, 73581-026 — Fexofenadine Hydrochloride, 73581-027 — FEXOFENADINE HYDROCHLORIDE, 73581-103 — FEXOFENADINE HYDROCHLORIDE, 73629-008 — Fexofenadine Hydrochloride, 77771-201 — fexofenadine hcl, 77771-202 — fexofenadine hcl, +225 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels