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
- 69230-300_eb46135f-d536-4328-96dc-30a2b16fe9d2
- Product NDC
- 69230-300
- Form
- TABLET
- Composition / generic term
- Fexofenadine HCL
- Labeler
- Camber Consumer Care
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160819
- Source listing expiry
- 20261231
Source-listed ingredients
- FEXOFENADINE HYDROCHLORIDE — 180 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (69230-300-01) / 100 TABLET in 1 BOTTLE · 69230-300-01
- 500 TABLET in 1 BOTTLE (69230-300-05) · 69230-300-05
- 1 BOTTLE in 1 CARTON (69230-300-30) / 30 TABLET in 1 BOTTLE · 69230-300-30
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 →