Hydrocortisone
- Product NDC
- 72789-062
- 11-digit product format
- 727890062
- Labeler code
- 72789
- Product ID
- 72789-062_e610588f-b288-1596-e053-2995a90a6a7a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocortisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA207029
- Marketing category
- ANDA
- Marketing start
- 2017-07-07
- Marketing end
- 0000-00-00
- Substance
- HYDROCORTISONE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72789-062-01 | 72789006201 | 100 TABLET in 1 BOTTLE, PLASTIC (72789-062-01) | 100 tablet | 2020-03-30 | 0000-00-00 | No | No | Current |