Hydrocortisone
- Product NDC
- 70934-350
- 11-digit product format
- 709340350
- Labeler code
- 70934
- Product ID
- 70934-350_b09cc1e1-1378-6019-e053-2995a90a7f32
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocortisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA207029
- Marketing category
- ANDA
- Marketing start
- 2019-05-07
- Marketing end
- 0000-00-00
- Substance
- HYDROCORTISONE
- Active strength
- 10 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 |
|---|
| 70934-350-30 | 70934035030 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-350-30) | 30 tablet | 2019-05-07 | 0000-00-00 | No | No | Current |