prednisone
- Product NDC
- 50090-7219
- 11-digit product format
- 500907219
- Labeler code
- 50090
- Product ID
- 50090-7219_28290a6c-6b79-478e-a71b-a243a0605d11
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA208412
- Marketing category
- ANDA
- Marketing start
- 2021-09-01
- 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 |
|---|
| 50090-7219-0 | 50090721900 | 60 TABLET in 1 BOTTLE (50090-7219-0) | 60 tablet | 2024-08-13 | No | No | Historical |
| 50090-7219-1 | 50090721901 | 20 TABLET in 1 BOTTLE (50090-7219-1) | 20 tablet | 2024-08-13 | No | No | Historical |