Hydrocortisone
- Product NDC
- 70954-053
- 11-digit product format
- 709540053
- Labeler code
- 70954
- Product ID
- 70954-053_0d7e8e04-9149-4436-bad1-b700e253b7ab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocortisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ANI Pharmaceuticals, Inc.
- Application
- ANDA217881
- Marketing category
- ANDA
- Marketing start
- 2025-05-05
- Substance
- HYDROCORTISONE
- Active strength
- 10 mg/1
- 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
- Hydrocortisone
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HYDROCORTISONE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | WI4X0X7BPJ |
| Rxcui | 197782, 197783, 197787 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70954-053-10 | Hydrocortisone | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70954-053 | HYDROCORTISONE TABLET [ANI PHARMACEUTICALS, INC.] | 1 | Current NDC, 1 package rows | 20250507_0d7e8e04-9149-4436-bad1-b700e253b7ab.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70954-053-10 | 70954005310 | 100 TABLET in 1 BOTTLE (70954-053-10) | 100 tablet | 2025-05-05 | No | No | Historical |