United States · FDA National Drug Code directory
Allergy Relief
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
- 69842-914_de7c79d2-f103-48b3-9d1d-194e6132ef3b
- Product NDC
- 69842-914
- Form
- TABLET, FILM COATED
- Composition / generic term
- fexofenadine hydrochloride
- Labeler
- CVS Pharmacy
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250403
- 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 (69842-914-01) / 70 TABLET, FILM COATED in 1 BOTTLE · 69842-914-01
- 15 BLISTER PACK in 1 CARTON (69842-914-22) / 1 TABLET, FILM COATED in 1 BLISTER PACK · 69842-914-22
- 1 BOTTLE in 1 CARTON (69842-914-39) / 30 TABLET, FILM COATED in 1 BOTTLE · 69842-914-39
- 1 BOTTLE in 1 CARTON (69842-914-47) / 150 TABLET, FILM COATED in 1 BOTTLE (69842-914-00) · 69842-914-47
- 1 BOTTLE in 1 CARTON (69842-914-49) / 40 TABLET, FILM COATED in 1 BOTTLE · 69842-914-49
- 1 BOTTLE in 1 CARTON (69842-914-75) / 90 TABLET, FILM COATED in 1 BOTTLE · 69842-914-75
- 1 BOTTLE in 1 CARTON (69842-914-95) / 45 TABLET, FILM COATED in 1 BOTTLE · 69842-914-95
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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