Methylprednisolone Sodium Succinate
- Product NDC
- 70518-2942
- 11-digit product format
- 705182942
- Labeler code
- 70518
- Product ID
- 70518-2942_b43af3fa-f4cc-9240-e053-2a95a90af929
- 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
- 2020-11-15
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2942-0 | 70518294200 | 25 VIAL, SINGLE-DOSE in 1 TRAY (70518-2942-0) > 2 mL in 1 VIAL, SINGLE-DOSE | 2020-11-15 | 0000-00-00 | No | No | Current |