prednisone
- Product NDC
- 50090-6122
- 11-digit product format
- 500906122
- Labeler code
- 50090
- Product ID
- 50090-6122_4466f506-8a9b-4e9d-ac63-f3e9af2bac4c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA213386
- Marketing category
- ANDA
- Marketing start
- 2020-06-24
- Substance
- PREDNISONE
- Active strength
- 20 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 |
|---|
| 50090-6122-1 | 50090612201 | 10 TABLET in 1 BOTTLE (50090-6122-1) | 10 tablet | 2022-09-30 | No | No | Historical |
| 50090-6122-2 | 50090612202 | 21 TABLET in 1 BOTTLE (50090-6122-2) | 21 tablet | 2022-09-30 | No | No | Historical |
| 50090-6122-3 | 50090612203 | 30 TABLET in 1 BOTTLE (50090-6122-3) | 30 tablet | 2022-09-30 | No | No | Historical |
| 50090-6122-5 | 50090612205 | 100 TABLET in 1 BOTTLE (50090-6122-5) | 100 tablet | 2022-09-30 | No | No | Historical |
| 50090-6122-9 | 50090612209 | 18 TABLET in 1 BOTTLE (50090-6122-9) | 18 tablet | 2022-09-30 | No | No | Historical |