hydrocortisone
- Product NDC
- 71335-2918
- 11-digit product format
- 713352918
- Labeler code
- 71335
- Product ID
- 71335-2918_0c9854c3-18cc-4b0d-9267-04eb49108f8e
- 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 |
|---|
| 71335-2918-1 | 71335291801 | 118 mL in 1 BOTTLE (71335-2918-1) | 118 ml | 2025-10-28 | No | No | Historical |