Prednisolone 60722-5011
Product NDC
60722-5011- Manufacturer
- Zhejiang Xianju Pharmaceutical Co., Ltd.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 1, 2024
- Listing Expires
- December 31, 2027
- Application
- ANDA218083
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Prednisolone | 5 mg/1 |
Drug Class
Corticosteroid [EPC]Corticosteroid Hormone Receptor Agonists [MoA]Corticosteroid [EPC]
Packaging Options(2)
100 TABLET in 1 BOTTLE (60722-5011-0)
1000 TABLET in 1 BOTTLE (60722-5011-1)