Hydrocortisone
- Product NDC
- 71335-2954
- 11-digit product format
- 713352954
- Labeler code
- 71335
- Product ID
- 71335-2954_adab8b80-c11c-46da-8116-4b57ec0de5a9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocortisone
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA080706
- Marketing category
- ANDA
- Marketing start
- 2016-04-01
- Substance
- HYDROCORTISONE
- Active strength
- 25 mg/g
- 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 |
|---|
| 71335-2954-1 | 71335295401 | 1 TUBE in 1 CARTON (71335-2954-1) / 30 g in 1 TUBE | 1 tube | 2025-11-05 | No | No | Historical |