NDC 72205-081-30
Erlotinib Hydrochloride 100 mg/1
Erlotinib Hydrochloride · TABLET, FILM COATED
Erlotinib Hydrochloride is a tablet, film coated containing erlotinib hydrochloride at a strength of 100 mg/1. Manufactured by Novadoz Pharmaceuticals LLC.
Key Facts
- Brand Name
- Erlotinib Hydrochloride
- Generic Name
- Erlotinib Hydrochloride
- NDC Code (Package)
72205-081-30- NDC Code (Product)
72205-081- Manufacturer
- Novadoz Pharmaceuticals LLC
- Strength
- 100 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA214366
- Marketing Start
- 05/11/2021
Recall History
No Recall HistoryView Full Drug Page
Erlotinib Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.