NDC 25021-821 – Methylprednisolone acetate

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

Human Prescription Drug 1 recall

Product NDC25021-821

Product details

Brand name
Methylprednisolone acetate
Generic name
Methylprednisolone acetate
Labeler
Sagent Pharmaceuticals
Dosage form
Injection, Suspension
Route
Intra-articular, Intralesional, Intramuscular, Intrasynovial, Soft Tissue
Marketing category
ANDA · ANDA201835
Marketed since
November 15, 2021
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
25021-821-051 VIAL in 1 CARTON (25021-821-05) / 5 mL in 1 VIALNov 15, 2021

Recalls mentioning this NDC

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