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
- 57344-292_1e038697-ba15-dca2-e063-6394a90a0bee
- Product NDC
- 57344-292
- Form
- TABLET
- Composition / generic term
- Fexofenadine Hydrochloride
- Labeler
- AAA PHARMACEUTICAL, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210706
- Source listing expiry
- 20261231
Source-listed ingredients
- FEXOFENADINE HYDROCHLORIDE — 180 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (57344-292-02) / 5 TABLET in 1 BLISTER PACK · 57344-292-02
- 1 BLISTER PACK in 1 CARTON (57344-292-03) / 5 TABLET in 1 BLISTER PACK · 57344-292-03
- 1 BOTTLE, PLASTIC in 1 CARTON (57344-292-04) / 30 TABLET in 1 BOTTLE, PLASTIC · 57344-292-04
- 1 BOTTLE, PLASTIC in 1 CARTON (57344-292-06) / 45 TABLET in 1 BOTTLE, PLASTIC · 57344-292-06
- 1 BOTTLE, PLASTIC in 1 CARTON (57344-292-17) / 30 TABLET in 1 BOTTLE, PLASTIC · 57344-292-17
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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