# Labetalol Hydrochloride

NDC: 60687-461
Generic name: Labetalol Hydrochloride
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20190716

FDA application: ANDA207743

## Active ingredients

- LABETALOL HYDROCHLORIDE: 300 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60687-461"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-461
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3004aa59-288c-4971-b77b-78789715ef5a