# PHENYLEPHRINE HYDROCHLORIDE

NDC: 71288-807
Generic name: PHENYLEPHRINE HYDROCHLORIDE
Labeler / Manufacturer: Meitheal Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20180427

FDA application: ANDA210334

## 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:"71288-807"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71288-807
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f2096e12-cbeb-4084-9132-17c7ef46b7b9