# Labetalol Hydrochloride

NDC: 29300-253
Generic name: Labetalol Hydrochloride
Labeler / Manufacturer: Unichem Pharmaceuticals (USA), Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20221001

FDA application: ANDA212719

## Active ingredients

- LABETALOL HYDROCHLORIDE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"29300-253"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=29300-253
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ed0188ba-3fd3-4680-a829-ba242a115fab