Fexofenadine HCl and Pseudoephedrine HCI

NDC 43598-823 · Dr. Reddy's Laboratories Inc.

Generic nameFexofenadine HCl and Pseudoephedrine HCI

Dosage formTABLET, 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

43598-823-14 — 4 BLISTER PACK in 1 CARTON (43598-823-14) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

43598-823-31 — 6 BLISTER PACK in 1 CARTON (43598-823-31) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

43598-823-35 — 2 BLISTER PACK in 1 CARTON (43598-823-35) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

41415-995 — fexofenadine hydrochloride and pseudoephedrine hydrochloride, 41520-229 — fexofenadine hcl, 41520-429 — Pseudoephedrine HCl, 41520-881 — Pseudoephedrine HCl, 42192-607 — Brompheniramine Maleate, Pseudoephedrine Hydrochloride, and Dextromethorphan Hydrobromide, 42192-630 — Brompheniramine Maleate, Pseudoephedrine Hydrochloride, and Dextromethorphan Hydrobromide, 42507-054 — Pseudoephedrine Hydrochloride, 42507-192 — Fexofenadine Hydrochloride, 42507-847 — fexofenadine hydrochloride, 43598-809 — Fexofenadine hydrochloride, 43598-892 — Fexofenadine HCl and Pseudoephedrine HCl, 43598-936 — Fexofenadine hydrochloride, 45802-107 — Pseudoephedrine HCl, 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, +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