# IBUPROFEN

NDC: 29485-9291
Generic name: IBUPROFEN 200MG
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: 20170502
Marketing ended: 20270618
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:"29485-9291"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=29485-9291
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8fc65767-1783-4f7f-8680-9e43ba4d5481