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
- 69168-475_1307fce8-d753-4df5-90f0-a902befdfe35
- Product NDC
- 69168-475
- Form
- TABLET
- Composition / generic term
- Loratadine 10mg
- Labeler
- Allegiant Health
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250318
- Source listing expiry
- 20261231
Source-listed ingredients
- LORATADINE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 150 TABLET in 1 BOTTLE (69168-475-02) · 69168-475-02
- 500 TABLET in 1 BOTTLE (69168-475-05) · 69168-475-05
- 1 BLISTER PACK in 1 CARTON (69168-475-08) / 5 TABLET in 1 BLISTER PACK · 69168-475-08
- 1 BLISTER PACK in 1 CARTON (69168-475-09) / 10 TABLET in 1 BLISTER PACK · 69168-475-09
- 300 TABLET in 1 BOTTLE (69168-475-17) · 69168-475-17
- 1 BOTTLE in 1 CARTON (69168-475-30) / 30 TABLET in 1 BOTTLE · 69168-475-30
- 60 TABLET in 1 BOTTLE (69168-475-60) · 69168-475-60
- 365 TABLET in 1 BOTTLE (69168-475-99) · 69168-475-99
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 →