NDC 0143-9850 – Methylprednisolone Sodium Succinate
Methylprednisolone Sodium Succinate 500 mg/1 · Injection, Powder, For Solution · Intramuscular, Intravenous
Product NDC0143-9850
Product details
- Brand name
- Methylprednisolone Sodium Succinate
- Generic name
- Methylprednisolone Sodium Succinate
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Dosage form
- Injection, Powder, For Solution
- Route
- Intramuscular, Intravenous
- Marketing category
- ANDA · ANDA202691
- Marketed since
- January 1, 2016
- Listing expires
- December 31, 2027
- Pharmacologic class
- Corticosteroid
Active ingredients
- Methylprednisolone Sodium Succinate 500 mg/1
Uses, dosage, side effects and warnings for Methylprednisolone Sodium Succinate →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0143-9850-01 | 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, MULTI-DOSE (0143-9850-01) | Jan 1, 2016 |
Recalls mentioning this NDC
- D-0801-2020 Jan 29, 2020 · Class III
Labeling: Incorrect Instructions: Vial label incorrectly instructs healthcare professional to reconstitute product with 16 mL rather than the correct volume of 8 mL of Bacteriostatic Water for…
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