Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride

NDC 47335-724 · Sun Pharmaceutical Industries, Inc.

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

47335-724-64 6 BLISTER PACK in 1 CARTON (47335-724-64) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (47335-724-60)

47335-724-66 2 BLISTER PACK in 1 CARTON (47335-724-66) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (47335-724-60)

47335-724-75 4 BLISTER PACK in 1 CARTON (47335-724-75) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (47335-724-60)

47335-724-83 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-724-83)

47335-724-94 1 BLISTER PACK in 1 CARTON (47335-724-94) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

47335-724-95 3 BLISTER PACK in 1 CARTON (47335-724-95) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

47335-724-99 2 BLISTER PACK in 1 CARTON (47335-724-99) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

45802-147 — Cetirizine hydrochloride, Pseudoephedrine hydrochloride, 45802-432 — Pseudoephedrine HCl, 45802-847 — fexofenadine hydrochloride, 46122-428 — Pseudoephedrine HCl, 46122-452 — Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, 46122-609 — Ibuprofen and Pseudoephedrine HCl, 46122-626 — Cetirizine hydrochloride, Pseudoephedrine hydrochloride, 46122-694 — Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, 46122-779 — FEXOFENADINE HYDROCHLORIDE, 46122-801 — Guaifenesin and Pseudoephedrine HCl, 49035-208 — Fexofenadine HCL, 49035-261 — Guaifenesin and Pseudoephedrine HCL, 49035-366 — fexofenadine hydrochloride, 49035-508 — pseudoephedrine hydrochloride, 49035-780 — Pseudoephedrine HCl, 50090-1075 — Guaifenesin and Pseudoephedrine Hydrochloride, 50090-1076 — Guaifenesin and Pseudoephedrine Hydrochloride, 50090-1203 — fexofenadine hydrochloride and pseudoephedrine hydrochloride, 50090-1234 — fexofenadine hydrochloride, 50090-1961 — Pseudoephedrine HCl, +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