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
- 62207-787_3b4cd1e9-fe92-7333-e063-6294a90af3f5
- Product NDC
- 62207-787
- Form
- TABLET
- Composition / generic term
- Loratadine
- Labeler
- Granules India Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200108
- Source listing expiry
- 20261231
Source-listed ingredients
- LORATADINE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE (62207-787-49) · 62207-787-49
- 5 POUCH in 1 BOX (62207-787-88) / 20000 TABLET in 1 POUCH · 62207-787-88
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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