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
- 41250-612_017c050c-5439-4d0c-8657-634901ea4439
- Product NDC
- 41250-612
- Form
- TABLET
- Composition / generic term
- Loratadine
- Labeler
- Meijer Distribution Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070418
- 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 (41250-612-03) / 70 TABLET in 1 BOTTLE · 41250-612-03
- 30 BLISTER PACK in 1 CARTON (41250-612-39) / 1 TABLET in 1 BLISTER PACK · 41250-612-39
- 40 BLISTER PACK in 1 CARTON (41250-612-49) / 1 TABLET in 1 BLISTER PACK · 41250-612-49
- 1 BOTTLE in 1 CARTON (41250-612-58) / 40 TABLET in 1 BOTTLE · 41250-612-58
- 1 BOTTLE in 1 CARTON (41250-612-65) / 30 TABLET in 1 BOTTLE · 41250-612-65
- 1 BOTTLE in 1 CARTON (41250-612-76) / 120 TABLET in 1 BOTTLE · 41250-612-76
- 1 BOTTLE in 1 CARTON (41250-612-87) / 300 TABLET in 1 BOTTLE · 41250-612-87
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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