NDC 17856-0815 – Prednisolone Sodium Phosphate

Prednisolone Sodium Phosphate 15 mg/5mL · Solution · Oral

Human Prescription Drug

Product NDC17856-0815

Product details

Brand name
Prednisolone Sodium Phosphate
Generic name
Prednisolone Sodium Phosphate
Labeler
ATLANTIC BIOLOGICALS CORP.
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA203559
Marketed since
October 9, 2023
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for PrednisoLONE Sodium Phosphate →

Package NDC codes (4)

Package NDCDescriptionSince
17856-0815-172 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0815-1) / 5 mL in 1 CUP, UNIT-DOSEJan 15, 2025
17856-0815-272 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0815-2) / 10 mL in 1 CUP, UNIT-DOSEJan 15, 2025
17856-0815-348 SYRINGE in 1 BOX, UNIT-DOSE (17856-0815-3) / 5 mL in 1 SYRINGEJan 15, 2025
17856-0815-545 SYRINGE in 1 BOX, UNIT-DOSE (17856-0815-5) / 5 mL in 1 SYRINGESep 4, 2026

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