# phenylephrine hydrochloride

NDC: 68083-339
Generic name: phenylephrine hydrochloride
Labeler / Manufacturer: Gland Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20201021

FDA application: ANDA211920

## 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:"68083-339"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68083-339
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6486d284-5189-4000-aa7d-67150e84a7b2