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
- 46122-779_76ea7e25-e968-4c78-9eca-ac960ad55985
- Product NDC
- 46122-779
- Form
- TABLET, FILM COATED
- Composition / generic term
- FEXOFENADINE HYDROCHLORIDE
- Labeler
- AMERISOURCE BERGEN
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240514
- 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 (46122-779-58) / 5 TABLET, FILM COATED in 1 BLISTER PACK · 46122-779-58
- 1 BOTTLE in 1 CARTON (46122-779-61) / 30 TABLET, FILM COATED in 1 BOTTLE · 46122-779-61
- 1 BOTTLE in 1 CARTON (46122-779-66) / 90 TABLET, FILM COATED in 1 BOTTLE · 46122-779-66
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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