PredniSONE
- Product NDC
- 70518-2138
- 11-digit product format
- 705182138
- Labeler code
- 70518
- Product ID
- 70518-2138_e87ae33c-fb05-33b0-e053-2995a90ad6e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PredniSONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA087342
- Marketing category
- ANDA
- Marketing start
- 2019-06-12
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2138-0 | 70518213800 | 10 TABLET in 1 BOTTLE, PLASTIC (70518-2138-0) | 10 tablet | 2019-06-12 | 0000-00-00 | No | No | Current |
| 70518-2138-1 | 70518213801 | 30 TABLET in 1 BLISTER PACK (70518-2138-1) | 30 tablet | 2021-05-10 | 0000-00-00 | No | No | Current |
| 70518-2138-2 | 70518213802 | 100 TABLET in 1 BOTTLE, PLASTIC (70518-2138-2) | 100 tablet | 2022-04-03 | 0000-00-00 | No | No | Current |
| 70518-2138-3 | 70518213803 | 34 TABLET in 1 BOTTLE, PLASTIC (70518-2138-3) | 34 tablet | 2022-09-09 | 0000-00-00 | No | No | Current |