# Acetaminophen

NDC: 24201-110
Generic name: Acetaminophen
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20230301

FDA application: ANDA202605

## 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:"24201-110"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24201-110
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7243bf2c-2c44-4dff-8a9e-d788d31dca86