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Non-Drowsy Allergy Relief

NDC 11673-621 · TARGET CORPORATION

Generic nameFexofenadine hydrochloride
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

11673-621-01 — 1 BOTTLE in 1 CARTON (11673-621-01) / 150 TABLET in 1 BOTTLE

11673-621-15 — 3 BLISTER PACK in 1 CARTON (11673-621-15) / 5 TABLET in 1 BLISTER PACK

11673-621-30 — 1 BOTTLE in 1 CARTON (11673-621-30) / 30 TABLET in 1 BOTTLE

11673-621-50 — 150 TABLET in 1 BOTTLE (11673-621-50)

11673-621-70 — 1 BOTTLE in 1 CARTON (11673-621-70) / 70 TABLET in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0363-9760 — Fexofenadine HCL, 0363-9765 — Fexofenadine HCL, 0536-1431 — Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, 0536-1491 — fexofenadine hydrochloride, pseudoephedrine hydrochloride, 0615-8648 — FEXOFENADINE HYDROCHLORIDE, 0904-6711 — Fexofenadine hydrochloride, 0904-7050 — Fexofenadine HCl, 0904-7192 — fexofenadine hcl, 0904-7486 — fexofenadine hcl, 10202-229 — 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, 16714-899 — Fexofenadine HCL, +225 more

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