United States · FDA National Drug Code directory
FEXOFENADINE HYDROCHLORIDE
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
- 51660-998_5110b287-1464-50d9-e063-6394a90abe0f
- Product NDC
- 51660-998
- Form
- TABLET, FILM COATED
- Composition / generic term
- FEXOFENADINE HYDROCHLORIDE
- Labeler
- OHM LABORATORIES INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220429
- 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 in 1 CARTON (51660-998-30) / 30 TABLET, FILM COATED in 1 BOTTLE · 51660-998-30
- 1 BOTTLE in 1 CARTON (51660-998-55) / 150 TABLET, FILM COATED in 1 BOTTLE · 51660-998-55
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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