# Labetalol Hydrochloride

NDC: 72603-903
Generic name: Labetalol Hydrochloride
Labeler / Manufacturer: NorthStar Rx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260319

FDA application: ANDA074787

## 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:"72603-903"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-903
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5bd81a8a-a480-4c8d-bd4f-3158412e6a73