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
- 79481-0847_dfa09879-a814-421c-8ea8-09193bc1c09d
- Product NDC
- 79481-0847
- Form
- TABLET, FILM COATED
- Composition / generic term
- fexofenadine hydrochloride
- Labeler
- Meijer, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20211006
- Source listing expiry
- 20261231
Source-listed ingredients
- FEXOFENADINE HYDROCHLORIDE — 180 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 BLISTER PACK in 1 CARTON (79481-0847-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK · 79481-0847-0
- 1 BOTTLE in 1 CARTON (79481-0847-1) / 30 TABLET, FILM COATED in 1 BOTTLE · 79481-0847-1
- 1 BOTTLE in 1 CARTON (79481-0847-2) / 45 TABLET, FILM COATED in 1 BOTTLE · 79481-0847-2
- 1 BOTTLE in 1 CARTON (79481-0847-3) / 40 TABLET, FILM COATED in 1 BOTTLE · 79481-0847-3
- 1 BOTTLE in 1 CARTON (79481-0847-4) / 90 TABLET, FILM COATED in 1 BOTTLE · 79481-0847-4
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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