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Fexofenadine HCL

NDC 16714-899 · NorthStar RxLLC

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

16714-899-01 — 1 BOTTLE in 1 CARTON (16714-899-01) / 30 TABLET in 1 BOTTLE

16714-899-02 — 1 BOTTLE in 1 CARTON (16714-899-02) / 100 TABLET in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

11673-621 — Fexofenadine hydrochloride, 11673-767 — Fexofenadine HCL, 11822-0021 — Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, 11822-3698 — Fexofenadine hydrochloride, 11822-7388 — Fexofenadine HCl and Pseudoephedrine HCI, 11822-7652 — Fexofenadine HCl, 11822-7660 — Fexofenadine HCl, 11822-7661 — Fexofenadine HCl, 11822-7663 — Fexofenadine HCl, 11822-7664 — Fexofenadine HCl, 21130-405 — Fexofenadine HCl, 21130-451 — Fexofenadine Hydrochloride, 21130-769 — Fexofenadine HCL, 21130-784 — Fexofenadine hydrochloride, 21130-821 — Fexofenadine HCl, 30142-059 — Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, 30142-097 — Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, 30142-447 — Fexofenadine HCl and Pseudoephedrine HCI, 30142-611 — Fexofenadine HCl and Pseudoephedrine HCI, 30142-856 — 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