# Ibuprofen

NDC: 66715-9819
Generic name: Ibuprofen tablet, film-coated
Labeler / Manufacturer: Lil' Drug Store Products, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20140912

FDA application: ANDA075010

## 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:"66715-9819"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=66715-9819
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e5bf5e09-7d42-6314-e053-2a95a90a2325