HYDROCORTISONE
- Product NDC
- 72162-2018
- 11-digit product format
- 721622018
- Labeler code
- 72162
- Product ID
- 72162-2018_979ac481-5382-433a-bb0c-2f2c6f0a062b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrocortisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040646
- Marketing category
- ANDA
- Marketing start
- 2007-03-30
- Substance
- HYDROCORTISONE
- Active strength
- 20 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| WI4X0X7BPJ | HYDROCORTISONE | 50-23-7 | HYDROCORTISONE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2018-1 | 72162201801 | 100 TABLET in 1 BOTTLE (72162-2018-1) | 100 tablet | 2024-07-17 | No | No | Historical |