Erlotinib Hydrochloride 72205-0081
Product NDC
72205-0081- Manufacturer
- Novadoz Pharmaceuticals Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 11, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA214366
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Erlotinib Hydrochloride | 100 mg/1 |
Drug Class
Kinase Inhibitor [EPC]Protein Kinase Inhibitors [MoA]
Packaging Options(1)
1 BOTTLE in 1 CARTON (72205-081-30) / 30 TABLET, FILM COATED in 1 BOTTLE