# HydrALAZINE hydrochloride

NDC: 0641-6231
Generic name: HydrALAZINE hydrochloride
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20201218

FDA application: ANDA213667

## 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:"0641-6231"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0641-6231
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3f5f1204-d289-40e9-be84-a29352f64bfb