United States · FDA National Drug Code directory
fexofenadine hcl
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
- 71399-8659_48c50815-5149-7bba-e063-6294a90a714d
- Product NDC
- 71399-8659
- Form
- TABLET, FILM COATED
- Composition / generic term
- fexofenadine hcl
- Labeler
- AKRON PHARMA INC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20141226
- Source listing expiry
- 20271231
Source-listed ingredients
- FEXOFENADINE HYDROCHLORIDE — 60 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (71399-8659-1) · 71399-8659-1
- 500 TABLET, FILM COATED in 1 BOTTLE (71399-8659-5) · 71399-8659-5
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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