Methylprednisolone Sodium Succinate
- Product NDC
- 70518-3128
- 11-digit product format
- 705183128
- Labeler code
- 70518
- Product ID
- 70518-3128_c50fc07d-1d6e-d68e-e053-2995a90a2c3d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METHYLPREDNISOLONE SODIUM SUCCINATE
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040583
- Marketing category
- ANDA
- Marketing start
- 2021-06-17
- Marketing end
- 0000-00-00
- Substance
- METHYLPREDNISOLONE SODIUM SUCCINATE
- Active strength
- 125 mg/2mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3128-0 | 70518312800 | 25 VIAL, SINGLE-DOSE in 1 TRAY (70518-3128-0) > 2 mL in 1 VIAL, SINGLE-DOSE (70518-3128-1) | 2021-06-17 | 0000-00-00 | No | No | Current |