United States · FDA National Drug Code directory
Fexofenadine HCl
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
- 69230-202_09845f21-f05e-34b2-e063-6394a90a7677
- Product NDC
- 69230-202
- Form
- TABLET, FILM COATED
- Composition / generic term
- Fexofenadine HCl
- Labeler
- Camber Consumer Care
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150916
- 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 (69230-202-01) / 100 TABLET, FILM COATED in 1 BOTTLE · 69230-202-01
- 500 TABLET, FILM COATED in 1 BOTTLE (69230-202-05) · 69230-202-05
- 1000 TABLET, FILM COATED in 1 BOTTLE (69230-202-11) · 69230-202-11
- 1 BOTTLE in 1 CARTON (69230-202-30) / 30 TABLET, FILM COATED in 1 BOTTLE · 69230-202-30
- 1 BOTTLE in 1 CARTON (69230-202-45) / 45 TABLET, FILM COATED in 1 BOTTLE · 69230-202-45
- 1 BOTTLE in 1 CARTON (69230-202-60) / 60 TABLET, FILM COATED in 1 BOTTLE · 69230-202-60
- 1 BOTTLE in 1 CARTON (69230-202-90) / 90 TABLET, FILM COATED in 1 BOTTLE · 69230-202-90
Source and coverage
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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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