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
- 58602-878_683cb2ea-c913-48f4-8adc-2888da3b655e
- Product NDC
- 58602-878
- Form
- TABLET, FILM COATED
- Composition / generic term
- Fexofenadine Hydrochloride
- Labeler
- Aurohealth LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231013
- Source listing expiry
- 20271231
Source-listed ingredients
- FEXOFENADINE HYDROCHLORIDE — 180 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (58602-878-09) / 30 TABLET, FILM COATED in 1 BOTTLE · 58602-878-09
- 500 TABLET, FILM COATED in 1 BOTTLE (58602-878-40) · 58602-878-40
- 1 BLISTER PACK in 1 CARTON (58602-878-60) / 5 TABLET, FILM COATED in 1 BLISTER PACK · 58602-878-60
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.
Browse United States records →