United States · FDA National Drug Code directory
DYE-FREE 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
- 51660-755_51156462-921d-facf-e063-6294a90a89fe
- Product NDC
- 51660-755
- Form
- TABLET, CHEWABLE
- Composition / generic term
- LORATADINE
- Labeler
- Ohm Laboratories Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251202
- 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 (51660-755-02) / 8 TABLET, CHEWABLE in 1 BLISTER PACK · 51660-755-02
- 6 BLISTER PACK in 1 CARTON (51660-755-03) / 8 TABLET, CHEWABLE in 1 BLISTER PACK · 51660-755-03
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 →