# Loratadine 10 mg

NDC: 49483-732
Generic name: Loratadine Tablets USP, 10 mg
Labeler / Manufacturer: TIME CAP LABORATORIES, INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250125

FDA application: ANDA219223

## 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:"49483-732"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49483-732
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2c80ea14-8490-4d26-e063-6294a90aecf0