# All Day Allergy Relief

NDC: 21130-914
Generic name: Loratadine
Labeler / Manufacturer: Safeway, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230331
Marketing ended: 20270331
FDA application: ANDA075209

## 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:"21130-914"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=21130-914
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9e581ae1-d1e6-4038-86e8-fd0c5ab9878a