United States · FDA National Drug Code directory
Allergy Relief
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
- 37808-391_e051ce8b-3163-69b9-e053-2a95a90ab739
- Product NDC
- 37808-391
- Form
- TABLET
- Composition / generic term
- Fexofenadine Hydrochloride
- Labeler
- HEB
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220531
- Source listing expiry
- 20261231
Source-listed ingredients
- FEXOFENADINE HYDROCHLORIDE — 60 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (37808-391-02) / 12 TABLET in 1 BLISTER PACK · 37808-391-02
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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