# Labetalol hydrochloride

NDC: 50090-6778
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: 19980803

FDA application: ANDA075133

## 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:"50090-6778"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-6778
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=83a6e770-207a-46bc-992d-c1ad90d1006d