# PHENYLEPHRINE HYDROCHLORIDE

NDC: 31722-344
Generic name: PHENYLEPHRINE HYDROCHLORIDE
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20240510

FDA application: ANDA218110

## 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:"31722-344"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-344
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=744da574-dfc9-4a22-8983-2ee15be2ea84