# Phenylephrine Hydrochloride

NDC: 70069-591
Generic name: Phenylephrine Hydrochloride
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: INTRAVENOUS
Marketing started: 20250304

FDA application: ANDA215617

## Active ingredients

- PHENYLEPHRINE HYDROCHLORIDE: .1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-591"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-591
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=170e63f1-23f4-4839-ab89-b81832d94a56