United States · FDA National Drug Code directory
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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
- 0113-0847_5cd21fe5-5a25-4beb-a480-924996e65ee1
- Product NDC
- 0113-0847
- Form
- TABLET, FILM COATED
- Composition / generic term
- fexofenadine hydrochloride
- Labeler
- L. Perrigo Company
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210910
- 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 (0113-0847-22) / 1 TABLET, FILM COATED in 1 BLISTER PACK · 0113-0847-22
- 1 BOTTLE in 1 CARTON (0113-0847-39) / 30 TABLET, FILM COATED in 1 BOTTLE · 0113-0847-39
- 1 BOTTLE in 1 CARTON (0113-0847-47) / 150 TABLET, FILM COATED in 1 BOTTLE (0113-0847-00) · 0113-0847-47
- 1 BOTTLE in 1 CARTON (0113-0847-95) / 45 TABLET, FILM COATED in 1 BOTTLE · 0113-0847-95
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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