PredniSONE
- Product NDC
- 68151-0820
- 11-digit product format
- 681510820
- Labeler code
- 68151
- Product ID
- 68151-0820_a78d32c4-e825-4368-9838-7869c4dd89f8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PredniSONE
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA088703
- Marketing category
- ANDA
- Marketing start
- 1986-12-13
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
NDC, Effective, Action table| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|
| 68151-0820-8 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-ad1a-f424-e053-dadaa90a57ce | PredniSONE Tablets USP, 1 mg, 2.5 mg, 5 mg, 10 mg, 20 mg, and 50 mg, PredniSONE Oral Solution USP, 5 mg per 5 mL and PredniSONE Intensol™ Oral Solution (Concentrate), 5 mg per mL |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68151-0820-8 | PredniSONE | 1 mL in 1 CUP | SOLUTION | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-0820 | PREDNISONE SOLUTION [CARILION MATERIALS MANAGEMENT] | 2 | Legacy NDC, 1 package rows | 20151229_5b46fc91-dc0a-4049-a767-5efcb1839eea.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 68151-0820-8 | 68151082008 | 1 mL in 1 CUP | 1 ml | Historical |