Hydrocortisone sodium succinate
- Product NDC
- 70710-1907
- 11-digit product format
- 707101907
- Labeler code
- 70710
- Product ID
- 70710-1907_9e47e808-7310-4c61-ac62-595a5c357123
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocortisone sodium succinate
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA217191
- Marketing category
- ANDA
- Marketing start
- 2026-05-09
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Hydrocortisone sodium succinate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HYDROCORTISONE SODIUM SUCCINATE | 100 mg/2mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 50LQB69S1Z |
| Rxcui | 238755 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70710-1907-1 | Hydrocortisone sodium succinate | 1 in 1 CARTON | INJECTION | 1 | | 1 |
| 70710-1907-1 | Hydrocortisone sodium succinate | 2 mL in 1 VIAL | INJECTION | 2 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70710-1907-1 | 70710190701 | 1 VIAL in 1 CARTON (70710-1907-1) / 2 mL in 1 VIAL | 1 vial | 2026-05-09 | No | No | Current |