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Fexofenadine HCL

NDC 51655-854 · Northwind Health Company, LLC

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

51655-854-26 — 90 TABLET in 1 BOTTLE, PLASTIC (51655-854-26)

51655-854-52 — 30 TABLET in 1 BOTTLE, PLASTIC (51655-854-52)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51316-007 — Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, 51316-015 — Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, 51316-018 — Fexofenadine HCl and Pseudoephedrine HCl, 51316-183 — FEXOFENADINE HYDROCHLORIDE, 51316-260 — Fexofenadine HCl, 51316-767 — Fexofenadine HCL, 51316-768 — Fexofenadine HCL, 51316-800 — FEXOFENADINE HYDROCHLORIDE, 51316-801 — Fexofenadine HCl, 51655-231 — Fexofenadine HCl, 51660-037 — Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, 51660-998 — FEXOFENADINE HYDROCHLORIDE, 51672-2141 — FEXOFENADINE HYDROCHLORIDE, 53943-392 — Fexofenadine Hydrochloride, 54257-170 — FEXOFENADINE HYDROCHLORIDE, 55111-447 — Fexofenadine HCl and Pseudoephedrine HCI, 55111-557 — Fexofenadine HCl and Pseudoephedrine HCI, 55111-782 — Fexofenadine hydrochloride, 55111-783 — Fexofenadine hydrochloride, 55111-784 — Fexofenadine hydrochloride, +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