NDC 55150-314 – Methylprednisolone Acetate

Methylprednisolone Acetate 80 mg/mL · Injection, Suspension · Intra-articular, Intralesional, Intramuscular, Soft Tissue

Human Prescription Drug 1 recall

Product NDC55150-314

Product details

Brand name
Methylprednisolone Acetate
Generic name
Methylprednisolone Acetate
Labeler
Eugia US LLC
Dosage form
Injection, Suspension
Route
Intra-articular, Intralesional, Intramuscular, Soft Tissue
Marketing category
ANDA · ANDA211930
Marketed since
April 13, 2023
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Methylprednisolone acetate →

Package NDC codes (2)

Package NDCDescriptionSince
55150-314-011 VIAL, MULTI-DOSE in 1 CARTON (55150-314-01) / 5 mL in 1 VIAL, MULTI-DOSEApr 13, 2023
55150-314-2525 VIAL, MULTI-DOSE in 1 CARTON (55150-314-25) / 5 mL in 1 VIAL, MULTI-DOSEApr 13, 2023

Recalls mentioning this NDC

Other Methylprednisolone acetate products