PREDNISONE
- Product NDC
- 50090-4785
- 11-digit product format
- 500904785
- Labeler code
- 50090
- Product ID
- 50090-4785_d4a57e86-31a7-4bca-a64e-0642ae49f013
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA210525
- Marketing category
- ANDA
- Marketing start
- 2018-12-04
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 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 |
|---|
| 50090-4785-0 | 50090478500 | 20 TABLET in 1 BOTTLE (50090-4785-0) | 20 tablet | 2019-12-10 | 0000-00-00 | No | No | Current |
| 50090-4785-1 | 50090478501 | 12 TABLET in 1 BOTTLE (50090-4785-1) | 12 tablet | 2019-12-10 | 0000-00-00 | No | No | Current |
| 50090-4785-2 | 50090478502 | 6 TABLET in 1 BOTTLE (50090-4785-2) | 6 tablet | 2019-12-10 | 0000-00-00 | No | No | Current |
| 50090-4785-5 | 50090478505 | 14 TABLET in 1 BOTTLE (50090-4785-5) | 14 tablet | 2019-12-10 | 0000-00-00 | No | No | Current |
| 50090-4785-7 | 50090478507 | 15 TABLET in 1 BOTTLE (50090-4785-7) | 15 tablet | 2019-12-10 | 0000-00-00 | No | No | Current |