Prednisone 42708-0114
Product NDC
42708-0114- Manufacturer
- Qpharma, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 1, 1990
- Listing Expires
- December 31, 2026
- Application
- ANDA080356
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Prednisone | 5 mg/1 |
Drug Class
Corticosteroid [EPC]Corticosteroid Hormone Receptor Agonists [MoA]Corticosteroid [EPC]
Packaging Options(1)
21 TABLET in 1 BOTTLE (42708-114-21)