# Labetalol HCL

NDC: 50090-1290
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: 20120724

FDA application: ANDA200908

## Active ingredients

- LABETALOL HYDROCHLORIDE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-1290"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-1290
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=312dde0d-5147-483e-968f-4e0d46114176