Solu-Cortef
- Product NDC
- 55154-3942
- 11-digit product format
- 551543942
- Labeler code
- 55154
- Product ID
- 55154-3942_bc348e8f-69c8-4cf4-a685-324ee3ebde87
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrocortisone sodium succinate
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Cardinal Health 107, LLC
- 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 |
|---|
| 55154-3942-5 | Solu-Cortef | 5 in 1 BAG | INJECTION, POWDER, FOR SOLUTION | 5 | | 16 |
| 55154-3942-5 | Solu-Cortef | 2 mL in 1 VIAL, SINGLE-DOSE | INJECTION, POWDER, FOR SOLUTION | 2 | | 16 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| hydrocortisone sodium succinate | ACTIVE INGREDIENT | 50LQB69S1Z | SOLU-CORTEF (HYDROCORTISONE SODIUM SUCCINATE) INJECTION, POWDER, FOR SOLUTION [CARDINAL HEALTH] | 6 | |
| hydrocortisone | ACTIVE MOIETY | WI4X0X7BPJ | SOLU-CORTEF (HYDROCORTISONE SODIUM SUCCINATE) INJECTION, POWDER, FOR SOLUTION [CARDINAL HEALTH] | 6 | |
| benzyl alcohol | INACTIVE INGREDIENT | LKG8494WBH | SOLU-CORTEF (HYDROCORTISONE SODIUM SUCCINATE) INJECTION, POWDER, FOR SOLUTION [CARDINAL HEALTH] | 6 | |
| sodium phosphate, dibasic | INACTIVE INGREDIENT | GR686LBA74 | SOLU-CORTEF (HYDROCORTISONE SODIUM SUCCINATE) INJECTION, POWDER, FOR SOLUTION [CARDINAL HEALTH] | 6 | |
| SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS | INACTIVE INGREDIENT | KH7I04HPUU | SOLU-CORTEF (HYDROCORTISONE SODIUM SUCCINATE) INJECTION, POWDER, FOR SOLUTION [CARDINAL HEALTH] | 6 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55154-3942 | SOLU-CORTEF (HYDROCORTISONE SODIUM SUCCINATE) INJECTION, POWDER, FOR SOLUTION [CARDINAL HEALTH 107, LLC] | 15 | Current NDC, Legacy NDC, 2 package rows | 20250112_f5bb0854-a477-4e59-914b-eeeaef92a596.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-3942-5 | 55154394205 | 5 VIAL, SINGLE-DOSE in 1 BAG (55154-3942-5) / 2 mL in 1 VIAL, SINGLE-DOSE | 1955-04-27 | 0000-00-00 | No | No | Current |