PredniSONE
- Product NDC
- 50090-1455
- 11-digit product format
- 500901455
- Labeler code
- 50090
- Product ID
- 50090-1455_f62dd441-5ca3-4b74-b1cd-2d96cfb4f0e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PredniSONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA087801
- Marketing category
- ANDA
- Marketing start
- 1982-04-22
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1455-0 | 50090145500 | 30 TABLET in 1 BOTTLE (50090-1455-0) | 30 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |