# Phenylephrine hydrochloride

NDC: 42023-214
Generic name: Phenylephrine hydrochloride
Labeler / Manufacturer: Par Health USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20190717

FDA application: ANDA210025

## Active ingredients

- PHENYLEPHRINE HYDROCHLORIDE: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42023-214"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42023-214
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d92631a6-bae8-493b-b4df-c563346607a8