# EPINEPHRINE

NDC: 63323-696
Generic name: EPINEPHRINE
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAMUSCULAR, INTRAOCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20241121

FDA application: ANDA213708

## 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:"63323-696"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-696
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a6afb9e8-1db9-480c-8d31-58c5c870ca49