# Non-Drowsy Allergy Relief

NDC: 66715-8815
Generic name: loratadine tablet
Labeler / Manufacturer: Lil' Drug Store Products, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220506

FDA application: ANDA076471

## 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:"66715-8815"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=66715-8815
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=031fc3e5-b5eb-447c-e063-6294a90a13b5