Hydrocortisone
- Product NDC
- 63629-8335
- 11-digit product format
- 636298335
- Labeler code
- 63629
- Product ID
- 63629-8335_58397522-1615-483a-b68e-e3e5707f6584
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocortisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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 [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 63629-8335-1 | 63629833501 | 60 TABLET in 1 BOTTLE (63629-8335-1) | 60 tablet | 2020-07-15 | 0000-00-00 | No | No | Current |