# Ibuprofen

NDC: 36800-662
Generic name: Ibuprofen
Labeler / Manufacturer: TOPCO ASSOCIATES LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20241014

FDA application: ANDA202312

## Active ingredients

- IBUPROFEN: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"36800-662"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=36800-662
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1a00c85b-2ba5-32c3-e063-6294a90af148