Prednisolone
- Product NDC
- 50090-0655
- 11-digit product format
- 500900655
- Labeler code
- 50090
- Product ID
- 50090-0655_a9ebeb33-5622-43d1-a24c-6b112bfadf57
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisolone
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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 Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 50090-0655-0 | 50090065500 | 2 BOTTLE in 1 CARTON (50090-0655-0) > 120 mL in 1 BOTTLE | 2 bottle | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0655-1 | 50090065501 | 4 BOTTLE in 1 CARTON (50090-0655-1) > 60 mL in 1 BOTTLE | 4 bottle | 2018-12-22 | 0000-00-00 | No | No | Current |
| 50090-0655-2 | 50090065502 | 1 BOTTLE in 1 CARTON (50090-0655-2) > 240 mL in 1 BOTTLE | 1 bottle | 2018-11-29 | 0000-00-00 | No | No | Current |