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
- 69842-242_434285f9-116c-458e-a598-fcdcd7be2825
- Product NDC
- 69842-242
- Form
- TABLET
- Composition / generic term
- Loratadine
- Labeler
- CVS Pharmacy, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190826
- Source listing expiry
- 20271231
Source-listed ingredients
- LORATADINE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 BLISTER PACK in 1 CARTON (69842-242-09) / 10 TABLET in 1 BLISTER PACK · 69842-242-09
- 1 BOTTLE in 1 CARTON (69842-242-17) / 45 TABLET in 1 BOTTLE · 69842-242-17
- 1 BOTTLE in 1 CARTON (69842-242-19) / 90 TABLET in 1 BOTTLE · 69842-242-19
- 365 TABLET in 1 BOTTLE (69842-242-39) · 69842-242-39
- 2 BOTTLE in 1 CARTON (69842-242-45) / 120 TABLET in 1 BOTTLE · 69842-242-45
- 1 BOTTLE in 1 CARTON (69842-242-54) / 70 TABLET in 1 BOTTLE · 69842-242-54
- 1 BLISTER PACK in 1 CARTON (69842-242-60) / 5 TABLET in 1 BLISTER PACK · 69842-242-60
- 2 BLISTER PACK in 1 CARTON (69842-242-67) / 10 TABLET in 1 BLISTER PACK · 69842-242-67
- 1 BLISTER PACK in 1 CARTON (69842-242-83) / 10 TABLET in 1 BLISTER PACK · 69842-242-83
- 3 BLISTER PACK in 1 CARTON (69842-242-91) / 10 TABLET in 1 BLISTER PACK · 69842-242-91
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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