United States · FDA National Drug Code directory

members mark 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
68196-711_566fe04e-ac31-4aef-9ec2-25756f03fb53
Product NDC
68196-711
Form
TABLET
Composition / generic term
Loratadine
Labeler
Sam's West Inc
Marketing category
ANDA
Marketing start / end (source format)
20240311
Source listing expiry
20261231

Source-listed ingredients

  • LORATADINE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 2 BOTTLE in 1 PACKAGE (68196-711-79) / 200 TABLET in 1 BOTTLE · 68196-711-79
  • 200 TABLET in 1 BOTTLE (68196-711-82) · 68196-711-82

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 →