PredniSONE
- Product NDC
- 70518-1553
- 11-digit product format
- 705181553
- Labeler code
- 70518
- Product ID
- 70518-1553_ec6bf1c7-1492-54b7-e053-2995a90ad30a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PredniSONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA087342
- Marketing category
- ANDA
- Marketing start
- 2018-10-19
- 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 |
|---|
| 70518-1553-0 | 70518155300 | 10 TABLET in 1 BOTTLE, PLASTIC (70518-1553-0) | 10 tablet | 2018-10-19 | 0000-00-00 | No | No | Current |