# Labetalol Hydrochloride

NDC: 72572-350
Generic name: Labetalol Hydrochloride
Labeler / Manufacturer: Civica, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20191121

FDA application: ANDA075303

## Active ingredients

- LABETALOL HYDROCHLORIDE: 5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72572-350"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72572-350
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d7c53b1c-b6a5-482a-a7c8-7425d9cd9ef8