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Allergy Relief

NDC 69842-914 · CVS Pharmacy

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

Packages

69842-914-01 1 BOTTLE in 1 CARTON (69842-914-01) / 70 TABLET, FILM COATED in 1 BOTTLE

69842-914-22 15 BLISTER PACK in 1 CARTON (69842-914-22) / 1 TABLET, FILM COATED in 1 BLISTER PACK

69842-914-39 1 BOTTLE in 1 CARTON (69842-914-39) / 30 TABLET, FILM COATED in 1 BOTTLE

69842-914-47 1 BOTTLE in 1 CARTON (69842-914-47) / 150 TABLET, FILM COATED in 1 BOTTLE (69842-914-00)

69842-914-49 1 BOTTLE in 1 CARTON (69842-914-49) / 40 TABLET, FILM COATED in 1 BOTTLE

69842-914-75 1 BOTTLE in 1 CARTON (69842-914-75) / 90 TABLET, FILM COATED in 1 BOTTLE

69842-914-95 1 BOTTLE in 1 CARTON (69842-914-95) / 45 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69168-413 — Fexofenadine HCl, 69168-416 — Fexofenadine HCl, 69168-437 — Fexofenadine HCl, 69168-450 — Allergy Relief, 69230-201 — Fexofenadine HCl, 69230-202 — Fexofenadine HCl, 69230-300 — Fexofenadine HCL, 69230-301 — Fexofenadine HCL, 69842-052 — Fexofenadine hydrochloride, 69842-492 — Fexofenadine Hydrochloride, 69842-973 — FEXOFENADINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE, 69842-990 — Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, 70000-0586 — Fexofenadine Hydrochloride, 70000-0677 — Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, 70000-0725 — fexofenadine hydrochloride, 70000-0726 — Fexofenadine Hydrochloride, 70000-0772 — fexofenadine hydrochloride, pseudoephedrine hydrochloride, 70010-183 — Fexofenadine HCL, 70677-1009 — Fexofenadine hydrochloride, 70677-1010 — Fexofenadine Hydrochloride and Pseudoephedrine 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