United States · FDA National Drug Code directory
All Day 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
- 83324-146_eb859e8d-d4f6-4823-8ce8-fa51f6f2245e
- Product NDC
- 83324-146
- Form
- TABLET
- Composition / generic term
- Loratadine
- Labeler
- QUALITY CHOICE (Chain Drug Marketing Association)
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240731
- Source listing expiry
- 20261231
Source-listed ingredients
- LORATADINE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 BOX (83324-146-30) / 30 TABLET in 1 BOTTLE, PLASTIC · 83324-146-30
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 →