# LABETALOL HYDROCHLORIDE

NDC: 60760-784
Generic name: Labetalol Hydrochloride
Labeler / Manufacturer: ST. MARY'S MEDICAL PARK PHARMACY
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20221025

FDA application: ANDA211953

## Active ingredients

- LABETALOL HYDROCHLORIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60760-784"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60760-784
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ed2293f8-2b82-c3db-e053-2995a90ad46c