# Phenylephrine hydrochloride

NDC: 81284-211
Generic name: Phenylephrine hydrochloride
Labeler / Manufacturer: Provepharm Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20200812

FDA application: ANDA211081

## 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:"81284-211"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=81284-211
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e1d3881f-fa9e-4d68-8ef0-9e03435fc292