Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride

NDC 69842-990 · CVS Pharmacy

Generic nameFexofenadine Hydrochloride and Pseudoephedrine Hydrochloride

Dosage formTABLET, FILM COATED, EXTENDED RELEASE

RouteORAL

Active ingredient(s)FEXOFENADINE HYDROCHLORIDE, PSEUDOEPHEDRINE HYDROCHLORIDE

Strength60; 120 mg/1; mg/1

Pharmacologic classAdrenergic alpha-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-Adrenergic Agonist [EPC]

Marketing categoryANDA

Packages

69842-990-20 — 1 BLISTER PACK in 1 CARTON (69842-990-20) / 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

69842-990-30 — 1 BLISTER PACK in 1 CARTON (69842-990-30) / 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69230-301 — Fexofenadine HCL, 69452-478 — BROMPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HYDROCHLORIDE, and DEXTROMETHORPHAN HYDROBROMIDE, 69842-052 — Fexofenadine hydrochloride, 69842-092 — Ibuprofen and Pseudoephedrine HCl, 69842-095 — Guaifenesin 600 mg and Pseudoephedrine HCl 60 mg, 69842-211 — Guaifenesin and Pseudoephedrine HCL, 69842-415 — cetirizine hydrochloride, pseudoephedrine hydrochloride, 69842-492 — Fexofenadine Hydrochloride, 69842-914 — fexofenadine hydrochloride, 69842-973 — FEXOFENADINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE, 69842-994 — Cetirizine hydrochloride and pseudoephedrine hydrochloride, 70000-0002 — Pseudoephedrine HCl, 70000-0042 — Cetirizine hydrochloride, Pseudoephedrine hydrochloride, 70000-0475 — Pseudoephedrine Hydrochloride, 70000-0586 — Fexofenadine Hydrochloride, 70000-0601 — Pseudoephedrine Hydrochloride, 70000-0605 — Naproxen sodium, Pseudoephedrine HCl, 70000-0606 — Ibuprofen and Pseudoephedrine HCl, 70000-0656 — Pseudoephedrine hydrochloride, 70000-0677 — Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, +483 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