Pazopanib Hydrochloride 66828-0282
Product NDC
66828-0282- Manufacturer
- Novartis Pharma Produktions Gmbh
- Dosage Form
- Tablet, Film Coated
- Product Type
- Human Prescription Drug
- Marketing Start
- July 12, 2016
- Listing Expires
- December 31, 2026
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Pazopanib Hydrochloride | 200 mg/1 |
Packaging Options(1)
25000 TABLET, FILM COATED in 1 DRUM (66828-0282-1)