# Labetalol Hydrochloride

NDC: 68001-381
Generic name: Labetalol Hydrochloride
Labeler / Manufacturer: BluePoint Laboratories Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20190218

FDA application: ANDA207743

## Active ingredients

- LABETALOL HYDROCHLORIDE: 100 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-381"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-381
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=63ede355-42ec-4c52-a941-51e5f6b35ed6