# Labetalol Hydrochloride

NDC: 70377-060
Generic name: Labetalol Hydrochloride
Labeler / Manufacturer: Biocon Pharma Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20210527

FDA application: ANDA209603

## Active ingredients

- LABETALOL HYDROCHLORIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70377-060"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70377-060
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=27e4ab03-c17b-4268-912c-e45a5e8f8dd8