Prednisolone Sodium Phosphate
- Product NDC
- 50090-1411
- 11-digit product format
- 500901411
- Labeler code
- 50090
- Product ID
- 50090-1411_a8847e53-e406-4b2e-a780-b76cb2e44859
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisolone Sodium Phosphate
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075183
- Marketing category
- ANDA
- Marketing start
- 2003-03-26
- Marketing end
- 0000-00-00
- Substance
- PREDNISOLONE SODIUM PHOSPHATE
- Active strength
- 5 mg/5mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record