# HydrALAZINE Hydrochloride

NDC: 76282-309
Generic name: HydrALAZINE Hydrochloride
Labeler / Manufacturer: Exelan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20160520

FDA application: ANDA090255

## Active ingredients

- HYDRALAZINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76282-309"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76282-309
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=811831f9-a844-463a-874d-fb8407659f0b