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
- 36800-653_08f3ce32-81a9-f9d2-e063-6394a90ab17d
- Product NDC
- 36800-653
- Form
- TABLET
- Composition / generic term
- Fexofenadine Hydrochloride
- Labeler
- TOPCO ASSOCIATES LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210831
- 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 (36800-653-03) / 15 TABLET in 1 BLISTER PACK · 36800-653-03
- 1 BOTTLE, PLASTIC in 1 CARTON (36800-653-07) / 60 TABLET in 1 BOTTLE, PLASTIC · 36800-653-07
- 1 BOTTLE, PLASTIC in 1 CARTON (36800-653-11) / 150 TABLET in 1 BOTTLE, PLASTIC · 36800-653-11
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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