United States · FDA National Drug Code directory
FEXOFENADINE HYDROCHLORIDE
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
- 51316-800_e6bae65e-9f41-4976-bebd-c14e86da14cb
- Product NDC
- 51316-800
- Form
- TABLET
- Composition / generic term
- FEXOFENADINE HYDROCHLORIDE
- Labeler
- CVS PHARMACY, INC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220920
- Source listing expiry
- 20261231
Source-listed ingredients
- FEXOFENADINE HYDROCHLORIDE — 180 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (51316-800-08) / 180 TABLET in 1 BOTTLE · 51316-800-08
- 1 BLISTER PACK in 1 CARTON (51316-800-15) / 15 TABLET in 1 BLISTER PACK · 51316-800-15
- 1 BOTTLE in 1 CARTON (51316-800-30) / 30 TABLET in 1 BOTTLE · 51316-800-30
- 1 BOTTLE in 1 CARTON (51316-800-45) / 45 TABLET in 1 BOTTLE · 51316-800-45
- 1 BOTTLE in 1 CARTON (51316-800-70) / 70 TABLET in 1 BOTTLE · 51316-800-70
- 1 BOTTLE in 1 CARTON (51316-800-90) / 90 TABLET in 1 BOTTLE · 51316-800-90
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →