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Prednisolone TebutateDrug - Prednisolone Tebutate The trade name of the product as shown on the labeling.
Dosage -
INJECTABLE; INJECTION
Active Ingredient(s) -
Prednisolone Tebutate
Strength -
20MG/ML
Applicant -
STERIS
New Drug Application (NDA) Number -
083362
Product Number -
001
Therapeutic Equivalence (TE) Code -
Approval Date -
Feb 17, 1984
Reference Listed Drug (RLD) -
No
Type -
DISCN
Applicant Full Name -
Steris Laboratories Inc
Prednisolone Tebutate
Prednisolone Tebutate 20mg/ml Injectable; Injection
Prednisolone Sodium Phosphate Eq 15mg Base/5ml Solution; Oral Prednisolone Sodium Phosphate Eq 5mg Base/5ml Solution; Oral Prednisolone Sodium Phosphate Eq 15mg Base/5ml Solution; Oral Prednisolone Sodium Phosphate Eq 5mg Base/5ml Solution; Oral Sulfacetamide Sodium And Prednisolone Sodium Phosphate Eq 0.23% Phosphate;10% Solution/drops; Ophthalmic Sulfacetamide Sodium And Prednisolone Sodium Phosphate Eq 0.23% Phosphate;10% Solution/drops; Ophthalmic Sulster Eq 0.23% Phosphate;10% Solution/drops; Ophthalmic Vasocidin Eq 0.23% Phosphate;10% Solution/drops; Ophthalmic Hydeltra-tba 20mg/ml Injectable; Injection NewDrugInformation |