SOLU-MEDROL
- Product NDC
- 71872-7232
- 11-digit product format
- 718727232
- Labeler code
- 71872
- Product ID
- 71872-7232_fb3394e0-0f73-b3f1-e053-6394a90a33aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylprednisolone sodium succinate
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- NDA011856
- Marketing category
- NDA
- Marketing start
- 1959-04-02
- Substance
- METHYLPREDNISOLONE SODIUM SUCCINATE
- Active strength
- 125 mg/2mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| LEC9GKY20K | METHYLPREDNISOLONE SODIUM SUCCINATE | 2375-03-3 | METHYLPREDNISOLONE SODIUM SUCCINATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7232-1 | 71872723201 | 1 VIAL in 1 BAG (71872-7232-1) / 2 mL in 1 VIAL | 1 vial | 2020-11-17 | No | No | Historical |