Solu-Cortef
- Product NDC
- 84549-011
- 11-digit product format
- 845490011
- Labeler code
- 84549
- Product ID
- 84549-011_3a38d1c4-e75c-f6e9-e063-6394a90a888b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrocortisone sodium succinate
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- ProPharma Distribution
- Application
- NDA009866
- Marketing category
- NDA
- Marketing start
- 1955-04-27
- Substance
- HYDROCORTISONE SODIUM SUCCINATE
- Active strength
- 100 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Solu-Cortef
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HYDROCORTISONE SODIUM SUCCINATE | 100 mg/2mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 50LQB69S1Z |
| Rxcui | 105398, 238755 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84549-011-04 | Solu-Cortef | 2 mL in 1 VIAL, SINGLE-DOSE | INJECTION, POWDER, FOR SOLUTION | 2 | | 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 |
|---|
| 84549-011-04 | 84549001104 | 2 mL in 1 VIAL, SINGLE-DOSE (84549-011-04) | 2 ml | 2025-08-27 | No | No | Historical |