SOLU-MEDROL
- Product NDC
- 84549-039
- 11-digit product format
- 845490039
- Labeler code
- 84549
- Product ID
- 84549-039_463eae7b-ee0e-b775-e063-6394a90ae2c3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylprednisolone sodium succinate
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- ProPharma Distribution
- Application
- NDA011856
- Marketing category
- NDA
- Marketing start
- 1959-04-02
- Substance
- METHYLPREDNISOLONE SODIUM SUCCINATE
- Active strength
- 40 mg/mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SOLU-MEDROL
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METHYLPREDNISOLONE SODIUM SUCCINATE | 40 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | LEC9GKY20K |
| Rxcui | 207191, 311659 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84549-039-28 | SOLU-MEDROL | 1 mL in 1 VIAL | INJECTION, POWDER, FOR SOLUTION | 1 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84549-039-28 | 84549003928 | 1 mL in 1 VIAL (84549-039-28) | 1 ml | 2025-10-10 | No | No | Historical |