# EPINEPHRINE

NDC: 80830-1659
Generic name: epinephrine
Labeler / Manufacturer: Amneal Pharmaceuticals Private Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20251208

FDA application: ANDA218208

## Active ingredients

- EPINEPHRINE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80830-1659"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80830-1659
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=33fa2443-5c80-4967-98bb-f60d3144421c