Prednisone
- Product NDC
- 72789-413
- 11-digit product format
- 727890413
- Labeler code
- 72789
- Product ID
- 72789-413_2e818a28-a5bf-5c98-e063-6294a90a51f3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA211575
- Marketing category
- ANDA
- Marketing start
- 2019-11-15
- Substance
- PREDNISONE
- Active strength
- 5 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 |
|---|
| 72789-413-21 | 72789041321 | 21 TABLET in 1 BOTTLE, PLASTIC (72789-413-21) | 21 tablet | 2024-06-10 | No | No | Historical |
| 72789-413-30 | 72789041330 | 30 TABLET in 1 BOTTLE, PLASTIC (72789-413-30) | 30 tablet | 2024-07-08 | No | No | Historical |