NDC 0009-3475 – Depo-Medrol

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

Human Prescription Drug 3 recalls

Product NDC0009-3475

Product details

Brand name
Depo-Medrol
Generic name
Methylprednisolone acetate
Labeler
Pharmacia & Upjohn Company LLC
Dosage form
Injection, Suspension
Route
Intra-articular, Intralesional, Intramuscular, Soft Tissue
Marketing category
NDA · NDA011757
Marketed since
May 28, 1959
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Depo-Medrol →

Package NDC codes (2)

Package NDCDescriptionSince
0009-3475-011 VIAL, SINGLE-DOSE in 1 PACKAGE (0009-3475-01) / 1 mL in 1 VIAL, SINGLE-DOSEMay 28, 1959
0009-3475-0325 VIAL, SINGLE-DOSE in 1 PACKAGE (0009-3475-03) / 1 mL in 1 VIAL, SINGLE-DOSEMay 28, 1959

Recalls mentioning this NDC

Other Depo-Medrol products