# Phenylephrine Hydrochloride

NDC: 0641-6229
Generic name: Phenylephrine Hydrochloride
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20121218

FDA application: NDA203826

## 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:"0641-6229"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0641-6229
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c3f358dd-4a36-4808-9943-e01f88604be5