# Labetalol Hydrochloride

NDC: 68083-111
Generic name: Labetalol Hydrochloride
Labeler / Manufacturer: Gland Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20120419

FDA application: ANDA090699

## 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:"68083-111"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68083-111
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=48caf986-3126-48e1-afcd-16d65c9cfe00