# Loratadine

NDC: 70010-162
Generic name: Loratadine
Labeler / Manufacturer: Granules Pharmaceuticals Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200101

FDA application: ANDA210722

## Active ingredients

- LORATADINE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70010-162"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70010-162
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d15add22-bc2d-9730-e053-2a95a90acd3f