hydrocortisone
- Product NDC
- 63629-8668
- 11-digit product format
- 636298668
- Labeler code
- 63629
- Product ID
- 63629-8668_334e1c3c-2586-474d-92bb-a4092d43a549
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrocortisone
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA089074
- Marketing category
- ANDA
- Marketing start
- 2008-05-23
- Substance
- HYDROCORTISONE
- Active strength
- 25 mg/mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 63629-8668-1 | 63629866801 | 59 mL in 1 BOTTLE (63629-8668-1) | 59 ml | 2008-09-24 | No | No | Historical |