# LABETALOL HYDROCHLORIDE

NDC: 72888-468
Generic name: Labetalol Hydrochloride
Labeler / Manufacturer: Advagen Pharma Ltd
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250520

FDA application: ANDA211953

## 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:"72888-468"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72888-468
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=106a0959-5830-489f-ba60-afd4eb0fac36