# Phenylephrine Hydrochloride

NDC: 0781-9227
Generic name: Phenylephrine Hydrochloride
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20210217

FDA application: ANDA208905

## 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:"0781-9227"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-9227
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5788f8c6-f868-4b83-81dc-dc485d8716c0