# Verapamil Hydrochloride

NDC: 43066-031
Generic name: verapamil hydrochloride
Labeler / Manufacturer: Baxter Healthcare Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20200325

FDA application: ANDA213232

## Active ingredients

- VERAPAMIL HYDROCHLORIDE: 2.5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43066-031"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43066-031
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=03c5daf8-5399-4d89-a747-9a9d7667b6e4