NDC 25021-821 – Methylprednisolone acetate
Methylprednisolone Acetate 80 mg/mL · Injection, Suspension · Intra-articular, Intralesional, Intramuscular, Intrasynovial, Soft Tissue
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
- Methylprednisolone Acetate 80 mg/mL
Uses, dosage, side effects and warnings for Methylprednisolone acetate →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 25021-821-05 | 1 VIAL in 1 CARTON (25021-821-05) / 5 mL in 1 VIAL | Nov 15, 2021 |
Recalls mentioning this NDC
- D-0499-2024 May 22, 2024 · Class II
Presence of Particulate Matter: Potential for black particulates in the drug product.
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