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
- 69842-052_d9904925-6db2-afaf-c11b-8bbf25249c49
- Product NDC
- 69842-052
- Form
- TABLET
- Composition / generic term
- Fexofenadine hydrochloride
- Labeler
- CVS Health Corp.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110401
- Source listing expiry
- 20261231
Source-listed ingredients
- FEXOFENADINE HYDROCHLORIDE — 180 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 BLISTER PACK in 1 CARTON (69842-052-15) / 5 TABLET in 1 BLISTER PACK · 69842-052-15
- 1 CARTON in 1 CARTON (69842-052-18) / 180 TABLET in 1 CARTON · 69842-052-18
- 3 BLISTER PACK in 1 CARTON (69842-052-29) / 15 TABLET in 1 BLISTER PACK · 69842-052-29
- 1 BOTTLE in 1 CARTON (69842-052-30) / 30 TABLET in 1 BOTTLE · 69842-052-30
- 1 BOTTLE in 1 CARTON (69842-052-45) / 45 TABLET in 1 BOTTLE · 69842-052-45
- 1 BOTTLE in 1 CARTON (69842-052-70) / 70 TABLET in 1 BOTTLE · 69842-052-70
- 1 BOTTLE in 1 CARTON (69842-052-90) / 90 TABLET in 1 BOTTLE · 69842-052-90
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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