Prednisolone
- Product NDC
- 63629-1862
- 11-digit product format
- 636291862
- Labeler code
- 63629
- Product ID
- 63629-1862_6807861f-8a1b-411f-a339-c9ab406a41ec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisolone
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040401
- Marketing category
- ANDA
- Marketing start
- 2003-02-27
- Marketing end
- 0000-00-00
- Substance
- PREDNISOLONE
- Active strength
- 15 mg/5mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 63629-1862-1 | 63629186201 | 60 mL in 1 BOTTLE (63629-1862-1) | 60 ml | 2004-12-13 | 0000-00-00 | No | No | Current |