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
- 0904-7192_b1390973-4ac1-40c9-b0e1-c7a4d04c0ee4
- Product NDC
- 0904-7192
- Form
- TABLET, FILM COATED
- Composition / generic term
- fexofenadine hcl
- Labeler
- Major Pharmaceuticals
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210826
- Source listing expiry
- 20261231
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 (0904-7192-04) · 0904-7192-04
- 500 TABLET, FILM COATED in 1 BOTTLE (0904-7192-40) · 0904-7192-40
- 100 TABLET, FILM COATED in 1 BOTTLE (0904-7192-60) · 0904-7192-60
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →