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Prednisolone Sodium Phosphate - 60432-212-08 - (PREDNISOLONE SODIUM PHOSPHATE)

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Drug Information of Prednisolone Sodium Phosphate

Product NDC: 60432-212
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: 60432-212
Labeler Name: Morton Grove Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076895
Marketing Category: ANDA
Start Marketing Date: 20041004

Package Information of Prednisolone Sodium Phosphate

Package NDC: 60432-212-08
Package Description: 237 mL in 1 BOTTLE, PLASTIC (60432-212-08)

NDC Information of Prednisolone Sodium Phosphate

NDC Code 60432-212-08
Proprietary Name Prednisolone Sodium Phosphate
Package Description 237 mL in 1 BOTTLE, PLASTIC (60432-212-08)
Product NDC 60432-212
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PREDNISOLONE SODIUM PHOSPHATE
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20041004
Marketing Category Name ANDA
Labeler Name Morton Grove Pharmaceuticals, Inc.
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


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