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
- 59726-701_5edf087a-8956-4840-a1e9-e9cb6d0fcf77
- Product NDC
- 59726-701
- Form
- TABLET, COATED
- Composition / generic term
- Fexofenadine HCl
- Labeler
- P & L Development, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210820
- Source listing expiry
- 20271231
Source-listed ingredients
- FEXOFENADINE HYDROCHLORIDE — 180 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 BOX (59726-701-15) / 150 TABLET, COATED in 1 BOTTLE, PLASTIC · 59726-701-15
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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