# ibuprofen

NDC: 37808-023
Generic name: Ibuprofen
Labeler / Manufacturer: H E B
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20160301

FDA application: ANDA074937

## Active ingredients

- IBUPROFEN: 100 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"37808-023"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-023
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bbcfea51-4c57-4a2c-a0ac-2a189c5ff38a