Prednisolone Sodium Phosphate 17856-8815-01

Package NDC

17856-8815-01

Manufacturer: Atlantic Biologicals Corp
Dosage Form: Solution
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: October 9, 2023
Listing Expires: December 31, 2026
Application: ANDA203559

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Active Ingredients

Ingredient	Strength
Prednisolone Sodium Phosphate	15 mg/5mL

Drug Class

Corticosteroid Hormone Receptor Agonists [MoA]Corticosteroid [EPC]

Selected Package

17856-8815-01Selected

50 CUP, UNIT-DOSE in 1 CASE (17856-8815-1) / 5 mL in 1 CUP, UNIT-DOSE