Home > National Drug Code (NDC) > Prednisolone Sodium Phosphate Oral Solution

Prednisolone Sodium Phosphate Oral Solution - 0178-0582-01 - (Prednisolone Sodium Phosphate)

Alphabetical Index


Drug Information of Prednisolone Sodium Phosphate Oral Solution

Product NDC: 0178-0582
Proprietary Name: Prednisolone Sodium Phosphate Oral Solution
Non Proprietary Name: Prednisolone Sodium Phosphate
Active Ingredient(s): 25    mg/5mL & nbsp;   Prednisolone Sodium Phosphate
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Prednisolone Sodium Phosphate Oral Solution

Product NDC: 0178-0582
Labeler Name: Mission Pharmacal Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091396
Marketing Category: ANDA
Start Marketing Date: 20121001

Package Information of Prednisolone Sodium Phosphate Oral Solution

Package NDC: 0178-0582-01
Package Description: 30 mL in 1 BOTTLE (0178-0582-01)

NDC Information of Prednisolone Sodium Phosphate Oral Solution

NDC Code 0178-0582-01
Proprietary Name Prednisolone Sodium Phosphate Oral Solution
Package Description 30 mL in 1 BOTTLE (0178-0582-01)
Product NDC 0178-0582
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prednisolone Sodium Phosphate
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20121001
Marketing Category Name ANDA
Labeler Name Mission Pharmacal Company
Substance Name PREDNISOLONE SODIUM PHOSPHATE
Strength Number 25
Strength Unit mg/5mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Prednisolone Sodium Phosphate Oral Solution


General Information