PREDNISONE
- Product NDC
- 68071-3738
- 11-digit product format
- 680713738
- Labeler code
- 68071
- Product ID
- 68071-3738_3b2e141b-dd02-7182-e063-6394a90a5d3c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA215672
- Marketing category
- ANDA
- Marketing start
- 2022-03-28
- 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 |
|---|
| 68071-3738-1 | 68071373801 | 10 TABLET in 1 BOTTLE (68071-3738-1) | 10 tablet | 2025-01-21 | No | No | Historical |
| 68071-3738-4 | 68071373804 | 4 TABLET in 1 BOTTLE (68071-3738-4) | 4 tablet | 2025-07-30 | No | No | Historical |
| 68071-3738-6 | 68071373806 | 6 TABLET in 1 BOTTLE (68071-3738-6) | 6 tablet | 2024-12-05 | No | No | Historical |