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
- 59726-801_7206fbae-edb3-4c2a-bcc2-27f68e010b4a
- Product NDC
- 59726-801
- Form
- TABLET, COATED
- Composition / generic term
- Fexofenadine HCl
- Labeler
- P & L Development, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210820 / 20270630
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 (59726-801-03) / 1 TABLET, COATED in 1 BLISTER PACK · 59726-801-03
- 120 BLISTER PACK in 1 CARTON (59726-801-12) / 1 TABLET, COATED in 1 BLISTER PACK · 59726-801-12
- 15 BLISTER PACK in 1 CARTON (59726-801-15) / 1 TABLET, COATED in 1 BLISTER PACK · 59726-801-15
- 1 BOTTLE, PLASTIC in 1 BOX (59726-801-30) / 30 TABLET, COATED in 1 BOTTLE, PLASTIC · 59726-801-30
- 1 BOTTLE, PLASTIC in 1 BOX (59726-801-70) / 70 TABLET, COATED in 1 BOTTLE, PLASTIC · 59726-801-70
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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