United States · FDA National Drug Code directory
Loratadine
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
- 69230-322_4f169a54-c021-23db-e063-6294a90a422e
- Product NDC
- 69230-322
- Form
- SOLUTION
- Composition / generic term
- Loratadine
- Labeler
- Camber Consumer Care Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210507
- Source listing expiry
- 20271231
Source-listed ingredients
- LORATADINE — 5 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (69230-322-12) / 120 mL in 1 BOTTLE · 69230-322-12
- 1 BOTTLE in 1 CARTON (69230-322-24) / 240 mL in 1 BOTTLE · 69230-322-24
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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