# Ibuprofen

NDC: 37808-709
Generic name: Ibuprofen
Labeler / Manufacturer: H E B
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20060704

FDA application: ANDA077349

## 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:"37808-709"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-709
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=21567c0f-abba-4a40-a0b9-5ce49b3d9648