# Acetaminophen

NDC: 63323-434
Generic name: ACETAMINOPHEN
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20201206

FDA application: NDA204767

## Active ingredients

- ACETAMINOPHEN: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-434"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-434
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a0cece43-256e-4adc-92f8-11a0f473bb83