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

Prednisolone Sodium Phosphate - 65162-667-90 - (Prednisolone Sodium Phosphate)

Alphabetical Index


Drug Information of Prednisolone Sodium Phosphate

Product NDC: 65162-667
Proprietary Name: Prednisolone Sodium Phosphate
Non Proprietary Name: Prednisolone Sodium Phosphate
Active Ingredient(s): 15    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

Product NDC: 65162-667
Labeler Name: Amneal Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078345
Marketing Category: ANDA
Start Marketing Date: 20091201

Package Information of Prednisolone Sodium Phosphate

Package NDC: 65162-667-90
Package Description: 473 mL in 1 BOTTLE (65162-667-90)

NDC Information of Prednisolone Sodium Phosphate

NDC Code 65162-667-90
Proprietary Name Prednisolone Sodium Phosphate
Package Description 473 mL in 1 BOTTLE (65162-667-90)
Product NDC 65162-667
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prednisolone Sodium Phosphate
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20091201
Marketing Category Name ANDA
Labeler Name Amneal Pharmaceuticals
Substance Name PREDNISOLONE SODIUM PHOSPHATE
Strength Number 15
Strength Unit mg/5mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Prednisolone Sodium Phosphate


General Information