United States · FDA National Drug Code directory
ALLERGY
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
- 72288-716_d9dbef15-7535-4292-9ea1-2f2416a813b5
- Product NDC
- 72288-716
- Form
- TABLET, FILM COATED
- Composition / generic term
- fexofenadine hydrochloride
- Labeler
- Amazon.com Services LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260817
- Source listing expiry
- 20271231
Source-listed ingredients
- FEXOFENADINE HYDROCHLORIDE — 180 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 150 TABLET, FILM COATED in 1 BOTTLE (72288-716-00) · 72288-716-00
- 1 BOTTLE in 1 CARTON (72288-716-39) / 30 TABLET, FILM COATED in 1 BOTTLE (72288-716-02) · 72288-716-39
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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