prednisone
- Product NDC
- 50090-5816
- 11-digit product format
- 500905816
- Labeler code
- 50090
- Product ID
- 50090-5816_659c0c9a-53f9-4bee-8003-93bf8dd94265
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA209727
- Marketing category
- ANDA
- Marketing start
- 2021-09-01
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 5 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 |
|---|
| 50090-5816-6 | 50090581606 | 90 TABLET in 1 BOTTLE (50090-5816-6) | 90 tablet | 2021-10-18 | 0000-00-00 | No | No | Current |