# PHENYLEPHRINE HYDROCHLORIDE

NDC: 70069-802
Generic name: PHENYLEPHRINE HYDROCHLORIDE
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20210922

FDA application: ANDA213318

## Active ingredients

- PHENYLEPHRINE HYDROCHLORIDE: 50 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-802"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-802
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=90a3853e-49d6-4536-be72-82cc875bcf74