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
- 72090-010_2aa6e396-3103-48d1-bcd7-43b140549307
- Product NDC
- 72090-010
- Form
- TABLET
- Composition / generic term
- FEXOFENADINE HYDROCHLORIDE
- Labeler
- Pioneer Life Sciences, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231207
- Source listing expiry
- 20261231
Source-listed ingredients
- FEXOFENADINE HYDROCHLORIDE — 180 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET in 1 BOTTLE (72090-010-01) · 72090-010-01
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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