Prednisone
- Product NDC
- 50090-7023
- 11-digit product format
- 500907023
- Labeler code
- 50090
- Product ID
- 50090-7023_b2a00abf-3a97-4539-ab8f-be055e5971a4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040256
- Marketing category
- ANDA
- Marketing start
- 2002-07-12
- Substance
- PREDNISONE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| VB0R961HZT | PREDNISONE | 53-03-2 | PREDNISONE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7023-0 | 50090702300 | 100 BLISTER PACK in 1 CARTON (50090-7023-0) / 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2024-01-08 | No | No | Historical |