# Labetalol Hydrochloride

NDC: 58657-602
Generic name: Labetalol Hydrochloride
Labeler / Manufacturer: Method Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20191122

FDA application: ANDA075215

## Active ingredients

- LABETALOL: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"58657-602"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=58657-602
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=733d6e32-ac90-4796-bf25-9d5887c897a5