United States · FDA National Drug Code directory
Fexofenadine Hydrochloride and Pseudoephedrine 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
- 69842-990_f6c3f3ab-f5b1-40d1-8ca9-51f55b9c66a9
- Product NDC
- 69842-990
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
- Labeler
- CVS Pharmacy
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180301
- Source listing expiry
- 20261231
Source-listed ingredients
- FEXOFENADINE HYDROCHLORIDE — 60 mg/1
- PSEUDOEPHEDRINE HYDROCHLORIDE — 120 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (69842-990-20) / 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK · 69842-990-20
- 1 BLISTER PACK in 1 CARTON (69842-990-30) / 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK · 69842-990-30
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 →