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
- 37835-602_59dbbbcb-e1e3-79e9-e063-6394a90a5ad8
- Product NDC
- 37835-602
- Form
- TABLET
- Composition / generic term
- Fexofenadine Hydrochloride
- Labeler
- Bi-Mart
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201218
- Source listing expiry
- 20271231
Source-listed ingredients
- FEXOFENADINE HYDROCHLORIDE — 180 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET in 1 BOTTLE (37835-602-09) · 37835-602-09
- 45 TABLET in 1 BOTTLE (37835-602-45) · 37835-602-45
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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