Erlotinib 00093-7664
Product NDC
00093-7664- Manufacturer
- Teva Pharmaceuticals Usa, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 9, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA091059
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Erlotinib Hydrochloride | 150 mg/1 |
Drug Class
Kinase Inhibitor [EPC]Protein Kinase Inhibitors [MoA]
Packaging Options(1)
30 TABLET, FILM COATED in 1 BOTTLE (0093-7664-56)