United States · FDA National Drug Code directory

Fexofenadine hydrochloride

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
43598-809_b7a3db43-ce44-e0e8-a3a3-b9412da4de27
Product NDC
43598-809
Form
TABLET
Composition / generic term
Fexofenadine hydrochloride
Labeler
Dr. Reddy's Laboratories Inc.
Marketing category
ANDA
Marketing start / end (source format)
20181226
Source listing expiry
20261231

Source-listed ingredients

  • FEXOFENADINE HYDROCHLORIDE — 180 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (43598-809-18) / 180 TABLET in 1 BOTTLE · 43598-809-18
  • 1 BOTTLE in 1 CARTON (43598-809-90) / 90 TABLET in 1 BOTTLE · 43598-809-90

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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Fexofenadine hydrochloride — United States | Molindra Medicines