Hydrocortisone
- Product NDC
- 68071-2546
- 11-digit product format
- 680712546
- Labeler code
- 68071
- Product ID
- 68071-2546_cd3809fc-4282-f915-e053-2995a90a381e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocortisone
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA085025
- Marketing category
- ANDA
- Marketing start
- 2006-03-31
- Marketing end
- 0000-00-00
- Substance
- HYDROCORTISONE
- Active strength
- 25 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2546-2 | 68071254602 | 1 TUBE in 1 CARTON (68071-2546-2) > 20 g in 1 TUBE | 1 tube | 2021-09-30 | 0000-00-00 | No | No | Current |