Prednisone
- Product NDC
- 70518-2703
- 11-digit product format
- 705182703
- Labeler code
- 70518
- Product ID
- 70518-2703_d6e6269a-72bd-2b90-e053-2995a90a1b21
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040584
- Marketing category
- ANDA
- Marketing start
- 2020-04-21
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2703-0 | 70518270300 | 250 TABLET in 1 BOTTLE, PLASTIC (70518-2703-0) | 250 tablet | 2020-04-21 | 0000-00-00 | No | No | Current |