Indications
USE(S) Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
- runny nose
- itchy, watery eyes
- sneezing
- itching of the nose or throat
Pregnancy and breastfeeding
If pregnant or breast-feeding, ask a health professional before use.
Composition
- Active ingredients
- LORATADINE 1MG/ML
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- LORATADINE 10MG · TabletANDA076301-001 · Over the counter
- LORATADINE 10MG · TabletANDA210722-001 · Over the counter
- LORATADINE 5MG · Tablet, orally disintegratingANDA212795-001 · Over the counter
- LORATADINE 1MG/ML · SuspensionNDA021734-001 · Discontinued
- LORATADINE 1MG/ML · SyrupANDA075505-001 · Discontinued
- LORATADINE 10MG · TabletANDA076134-001 · Over the counter
- LORATADINE 1MG/ML · SyrupANDA077421-001 · Over the counter
- LORATADINE 1MG/ML · SyrupANDA075728-001 · Over the counter
- LORATADINE 10MG · Tablet, orally disintegratingANDA075990-001 · Discontinued
- LORATADINE 10MG · TabletANDA078447-001 · Discontinued
- LORATADINE 10MG · CapsuleANDA202538-001 · Over the counter
At a glance
- Brand name
- Loratadine
- Route
- Oral
- Dosage form
- Syrup
- Applicant
- Hetero Labs LTD III
- Status
- Over the counter
- FDA approval
- 7 May 2021
- Application
- ANDA210409-001