United States · FDA National Drug Code directory
Non-Drowsy 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
- 11673-621_d7eb1caf-eeff-10b7-c464-3592c8d7d0ee
- Product NDC
- 11673-621
- Form
- TABLET
- Composition / generic term
- Fexofenadine hydrochloride
- Labeler
- TARGET CORPORATION
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250801
- 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 (11673-621-01) / 150 TABLET in 1 BOTTLE · 11673-621-01
- 3 BLISTER PACK in 1 CARTON (11673-621-15) / 5 TABLET in 1 BLISTER PACK · 11673-621-15
- 1 BOTTLE in 1 CARTON (11673-621-30) / 30 TABLET in 1 BOTTLE · 11673-621-30
- 150 TABLET in 1 BOTTLE (11673-621-50) · 11673-621-50
- 1 BOTTLE in 1 CARTON (11673-621-70) / 70 TABLET in 1 BOTTLE · 11673-621-70
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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