# Ibuprofen

NDC: 76420-577
Generic name: Ibuprofen
Labeler / Manufacturer: Asclemed USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200508

FDA application: ANDA213794

## Active ingredients

- IBUPROFEN: 800 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76420-577"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76420-577
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=793e4b36-8208-4fa3-9f4f-9e9e72648280