PROCTOZONE-HC
- Product NDC
- 72162-1805
- 11-digit product format
- 721621805
- Labeler code
- 72162
- Product ID
- 72162-1805_6f7c466b-e390-434c-afdd-fa2a6f0af56e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrocortisone 2.5%
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040879
- Marketing category
- ANDA
- Marketing start
- 2015-08-03
- 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 |
|---|
| 72162-1805-2 | 72162180502 | 1 TUBE in 1 CARTON (72162-1805-2) / 30 g in 1 TUBE | 1 tube | 2023-10-04 | No | No | Historical |