United States · FDA National Drug Code directory
Loratadine 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
- 37808-529_c624b449-9db2-4b2e-852f-28f745aa7e2a
- Product NDC
- 37808-529
- Form
- TABLET
- Composition / generic term
- Loratadine
- Labeler
- HEB
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180201
- Source listing expiry
- 20261231
Source-listed ingredients
- LORATADINE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (37808-529-01) · 37808-529-01
- 1 BLISTER PACK in 1 CARTON (37808-529-11) / 10 TABLET in 1 BLISTER PACK · 37808-529-11
- 30 BLISTER PACK in 1 CARTON (37808-529-31) / 1 TABLET in 1 BLISTER PACK · 37808-529-31
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →