# hydrALAZINE Hydrochloride

NDC: 70518-3659
Generic name: hydrALAZINE Hydrochloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20230227

FDA application: ANDA040388

## Active ingredients

- HYDRALAZINE HYDROCHLORIDE: 20 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-3659"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-3659
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dca82025-a4cd-4856-aa19-bdf091bf8973