Hydrocortisone
- Product NDC
- 76420-031
- 11-digit product format
- 764200031
- Labeler code
- 76420
- Product ID
- 76420-031_a8e5cbe9-22a7-4051-e053-2995a90a93f7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocortisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA207029
- Marketing category
- ANDA
- Marketing start
- 2017-07-07
- Marketing end
- 0000-00-00
- Substance
- HYDROCORTISONE
- Active strength
- 5 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76420-031 | HYDROCORTISONE TABLET [ASCLEMED USA, INC.] | 1 | Legacy NDC | 20200626_beeb5009-ad7e-40cb-a127-99cff20d49dd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76420-031-50 | 76420003150 | 50 TABLET in 1 BOTTLE, PLASTIC (76420-031-50) | 50 tablet | 2020-06-25 | 0000-00-00 | No | No | Current |