# Labetalol Hydrochloride

NDC: 68001-702
Generic name: Labetalol Hydrochloride
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260604

FDA application: ANDA074787

## Active ingredients

- LABETALOL HYDROCHLORIDE: 300 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-702"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-702
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e4562c70-f245-4dbe-8fe1-0bb64a91a315