Prednisone
- Product NDC
- 55154-8130
- 11-digit product format
- 551548130
- Labeler code
- 55154
- Product ID
- 55154-8130_f5b7636e-20ff-463b-a90c-f6eff4240a5f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA085161
- Marketing category
- ANDA
- Marketing start
- 1990-01-01
- 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
- 2021-12-31
- 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 |
|---|
| 55154-8130-0 | 55154813000 | 10 BLISTER PACK in 1 BAG (55154-8130-0) > 1 TABLET in 1 BLISTER PACK | 10 blister pack | 1990-01-01 | 0000-00-00 | No | No | Current |