# Allergy Relief

NDC: 68998-414
Generic name: Loratadine
Labeler / Manufacturer: Marc Glassman, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200501

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:"68998-414"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68998-414
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=717ccb47-e13c-4464-b6e6-bea8f24d4663