United States · FDA National Drug Code directory
Loratadine 10mg
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
- 25000-092_aa667b5f-a4ac-4129-bae9-f9c1de776629
- Product NDC
- 25000-092
- Form
- TABLET
- Composition / generic term
- Loratadine 10mg
- Labeler
- MARKSANS PHARMA LIMITED
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241121
- Source listing expiry
- 20261231
Source-listed ingredients
- LORATADINE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (25000-092-03) / 30 TABLET in 1 BOTTLE · 25000-092-03
- 1 BOTTLE in 1 CARTON (25000-092-79) / 150 TABLET in 1 BOTTLE · 25000-092-79
- 365 TABLET in 1 BOTTLE (25000-092-80) · 25000-092-80
- 2 BLISTER PACK in 1 CARTON (25000-092-81) / 7 TABLET in 1 BLISTER PACK · 25000-092-81
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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