Prednisone
- Product NDC
- 0615-3593
- 11-digit product format
- 006153593
- Labeler code
- 0615
- Product ID
- 0615-3593_af8526b7-1429-456f-a6ef-dc0ba71401d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA084122
- Marketing category
- ANDA
- Marketing start
- 2003-02-13
- Marketing end
- 2022-11-30
- Substance
- PREDNISONE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- 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 |
|---|
| 0615-3593-05 | 00615359305 | 15 TABLET in 1 BLISTER PACK (0615-3593-05) | 15 tablet | 2018-11-12 | 2022-11-30 | No | No | Current |
| 0615-3593-30 | 00615359330 | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-3593-30) > 5 TABLET in 1 BLISTER PACK | 6 blister pack | 2014-11-14 | 2022-09-30 | No | No | Current |
| 0615-3593-39 | 00615359339 | 30 TABLET in 1 BLISTER PACK (0615-3593-39) | 30 tablet | 2013-01-10 | 2022-11-30 | No | No | Current |