NDC 70121-1001 – Methylprednisolone Sodium Succinate

Methylprednisolone Sodium Succinate 125 mg/2mL · Injection, Powder, Lyophilized, For Solution · Intramuscular, Intravenous

Human Prescription Drug

Product NDC70121-1001

Product details

Brand name
Methylprednisolone Sodium Succinate
Generic name
Methylprednisolone
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intramuscular, Intravenous
Marketing category
ANDA · ANDA207549
Marketed since
November 11, 2016
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Methylprednisolone Sodium Succinate →

Package NDC codes (1)

Package NDCDescriptionSince
70121-1001-525 VIAL in 1 CARTON (70121-1001-5) / 2 mL in 1 VIAL (70121-1001-1)Nov 11, 2016

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