# Phenylephrine Hydrochloride

NDC: 71839-129
Generic name: Phenylephrine Hydrochloride
Labeler / Manufacturer: BE Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20230710

FDA application: ANDA217521

## 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:"71839-129"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71839-129
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fb069778-d16e-40f9-9c02-5496adfcb5d2