Details for New Drug Application (NDA): 217881
The generic ingredient in HYDROCORTISONE is hydrocortisone valerate. There are seven drug master file entries for this compound. Five suppliers are listed for this compound. Additional details are available on the hydrocortisone valerate profile page.
Summary for 217881
| Tradename: | HYDROCORTISONE |
| Applicant: | Novitium Pharma |
| Ingredient: | hydrocortisone |
| Patents: | 0 |
Pharmacology for NDA: 217881
| Mechanism of Action | Corticosteroid Hormone Receptor Agonists |
Medical Subject Heading (MeSH) Categories for 217881
Suppliers and Packaging for NDA: 217881
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| HYDROCORTISONE | hydrocortisone | TABLET;ORAL | 217881 | ANDA | ANI Pharmaceuticals, Inc. | 70954-052 | 70954-052-10 | 50 TABLET in 1 BOTTLE (70954-052-10) |
| HYDROCORTISONE | hydrocortisone | TABLET;ORAL | 217881 | ANDA | ANI Pharmaceuticals, Inc. | 70954-053 | 70954-053-10 | 100 TABLET in 1 BOTTLE (70954-053-10) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 5MG | ||||
| Approval Date: | May 2, 2025 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
| Approval Date: | May 2, 2025 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 20MG | ||||
| Approval Date: | May 2, 2025 | TE: | AB | RLD: | No | ||||
Complete Access Available with Subscription
