# Ibuprofen

NDC: 37808-609
Generic name: Ibuprofen
Labeler / Manufacturer: HEB
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, LIQUID FILLED
Routes: ORAL
Marketing started: 20210924

FDA application: ANDA078682

## 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:"37808-609"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-609
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ca4be24c-5d92-ddc9-e053-2a95a90aa5a7