Prednisone
- Product NDC
- 72189-593
- 11-digit product format
- 721890593
- Labeler code
- 72189
- Product ID
- 72189-593_26194836-90ca-6909-e063-6294a90a6f98
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA209727
- Marketing category
- ANDA
- Marketing start
- 2024-11-04
- 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 |
|---|
| 72189-593-21 | 72189059321 | 21 TABLET in 1 BOTTLE (72189-593-21) | 21 tablet | 2024-11-04 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Prednisone | Direct_Rx | 2024-11-04 | HUMAN PRESCRIPTION DRUG LABEL | 1 |