# Gefitinib

NDC: 50742-366
Generic name: Gefitinib
Labeler / Manufacturer: Ingenus Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20230427

FDA application: ANDA211591

## Active ingredients

- GEFITINIB: 250 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50742-366"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50742-366
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6402435f-9f6a-4f02-91a2-6267d783fa78