# HYDRALAZINE HYDROCHLORIDE

NDC: 51662-1648
Generic name: HYDRALAZINE HYDROCHLORIDE
Labeler / Manufacturer: HF Acquisition Co LLC, DBA HealthFirst
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 19970630

FDA application: ANDA040136

## 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:"51662-1648"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1648
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=15b0f03b-b5a2-c49d-e063-6394a90a5b15