PredniSONE
- Product NDC
- 0615-8307
- 11-digit product format
- 006158307
- Labeler code
- 0615
- Product ID
- 0615-8307_0d4f8c24-4daa-4881-81da-0502deba0fd2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PredniSONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA087342
- Marketing category
- ANDA
- Marketing start
- 2003-02-13
- Marketing end
- 2024-07-31
- Substance
- PREDNISONE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0615-8307-39 | 00615830739 | 30 TABLET in 1 BLISTER PACK (0615-8307-39) | 30 tablet | 2019-07-02 | 2024-07-31 | No | No | Current |