United States · FDA National Drug Code directory

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
72036-193_c11dbffc-c6b2-a259-e053-2a95a90a9f31
Product NDC
72036-193
Form
TABLET
Composition / generic term
Loratadine
Labeler
HARRIS TEETER
Marketing category
ANDA
Marketing start / end (source format)
20210125
Source listing expiry
20261231

Source-listed ingredients

  • LORATADINE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BLISTER PACK in 1 CARTON (72036-193-04) / 10 TABLET in 1 BLISTER PACK · 72036-193-04
  • 1 BOTTLE, PLASTIC in 1 CARTON (72036-193-06) / 30 TABLET in 1 BOTTLE, PLASTIC · 72036-193-06
  • 1 BOTTLE, PLASTIC in 1 CARTON (72036-193-11) / 90 TABLET in 1 BOTTLE, PLASTIC · 72036-193-11

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 →