# IBUPROFEN

NDC: 49483-601
Generic name: IBUPROFEN
Labeler / Manufacturer: TIME CAP LABORATORIES,INC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160322

FDA application: ANDA091239

## 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:"49483-601"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49483-601
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f58d35f9-e44b-417b-98ce-0766b537cd2f