# Erlotinib

NDC: 72485-218
Generic name: Erlotinib hydrochloride
Labeler / Manufacturer: Armas Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20191106

FDA application: ANDA211960

## Active ingredients

- ERLOTINIB HYDROCHLORIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72485-218"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72485-218
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2c4c7353-b81c-4651-8aac-6d15e88145af