# LABETALOL HYDROCHLORIDE

NDC: 50090-7666
Generic name: Labetalol Hydrochloride
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20210818

FDA application: ANDA211953

## Active ingredients

- LABETALOL HYDROCHLORIDE: 300 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-7666"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-7666
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fffb7c59-ad92-4e74-850d-d94d42b7fdc9