prednisone
- Product NDC
- 68788-8663
- 11-digit product format
- 687888663
- Labeler code
- 68788
- Product ID
- 68788-8663_56c6804b-c88c-445c-a8a0-b90ec12166bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA208412
- Marketing category
- ANDA
- Marketing start
- 2024-05-13
- 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 |
|---|
| 68788-8663-1 | 68788866301 | 10 TABLET in 1 BOTTLE, PLASTIC (68788-8663-1) | 10 tablet | 2024-05-13 | No | No | Historical |
| 68788-8663-2 | 68788866302 | 20 TABLET in 1 BOTTLE, PLASTIC (68788-8663-2) | 20 tablet | 2024-05-13 | No | No | Historical |
| 68788-8663-3 | 68788866303 | 30 TABLET in 1 BOTTLE, PLASTIC (68788-8663-3) | 30 tablet | 2024-05-13 | No | No | Historical |
| 68788-8663-4 | 68788866304 | 18 TABLET in 1 BOTTLE, PLASTIC (68788-8663-4) | 18 tablet | 2024-05-13 | No | No | Historical |
| 68788-8663-5 | 68788866305 | 15 TABLET in 1 BOTTLE, PLASTIC (68788-8663-5) | 15 tablet | 2024-05-13 | No | No | Historical |
| 68788-8663-8 | 68788866308 | 21 TABLET in 1 BOTTLE, PLASTIC (68788-8663-8) | 21 tablet | 2024-05-13 | No | No | Historical |