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Prednisolone - 0093-6118-87 - (Prednisolone)

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Drug Information of Prednisolone

Product NDC: 0093-6118
Proprietary Name: Prednisolone
Non Proprietary Name: Prednisolone
Active Ingredient(s): 15    mg/5mL & nbsp;   Prednisolone
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Prednisolone

Product NDC: 0093-6118
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089081
Marketing Category: ANDA
Start Marketing Date: 19981211

Package Information of Prednisolone

Package NDC: 0093-6118-87
Package Description: 240 mL in 1 BOTTLE (0093-6118-87)

NDC Information of Prednisolone

NDC Code 0093-6118-87
Proprietary Name Prednisolone
Package Description 240 mL in 1 BOTTLE (0093-6118-87)
Product NDC 0093-6118
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prednisolone
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 19981211
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name PREDNISOLONE
Strength Number 15
Strength Unit mg/5mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Prednisolone


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