Fexofenadine HCl and Pseudoephedrine HCI

NDC 55111-447 · Dr. Reddy's Laboratories Limited

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

55111-447-14 — 4 BLISTER PACK in 1 CARTON (55111-447-14) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (55111-447-07)

55111-447-31 — 6 BLISTER PACK in 1 CARTON (55111-447-31) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (55111-447-07)

55111-447-35 — 2 BLISTER PACK in 1 CARTON (55111-447-35) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (55111-447-07)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51672-2141 — FEXOFENADINE HYDROCHLORIDE, 53943-204 — Pseudoephedrine hydrochloride, 53943-392 — Fexofenadine Hydrochloride, 54257-170 — FEXOFENADINE HYDROCHLORIDE, 54859-502 — Dextromethorphan, Guiafenesin, Pseudoephedrine HCl, 54859-514 — Dextromethorphan HBr, Pseufoephedrine HCl, Triprolidine HCl, 54859-544 — Dextromethorphan, Guiafenesin, Pseudoephedrine HCl, 54859-603 — Dextromethorphan, Guiafenesin, Pseudoephedrine HCl, 54859-803 — Dexbrompheniramine Maleate, Pseudoephedrine HCl, 54859-812 — Dexbrompheniramine Maleate, Pseudoephedrine HCl, 55111-557 — Fexofenadine HCl and Pseudoephedrine HCI, 55111-782 — Fexofenadine hydrochloride, 55111-783 — Fexofenadine hydrochloride, 55111-784 — Fexofenadine hydrochloride, 55111-798 — Guaifenesin and Pseudoephedrine HCL, 55111-799 — Guaifenesin and Pseudoephedrine HCL, 55301-847 — fexofenadine hydrochloride, 55319-917 — Fexofenadine hydrochloride, 55319-923 — Fexofenadine HCl, 55319-957 — Fexofenadine 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