Hydrocortisone Acetate
- Product NDC
- 69367-260
- 11-digit product format
- 693670260
- Labeler code
- 69367
- Product ID
- 69367-260_27e6ec88-81d3-47d2-94d0-7fe6e2265237
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocortisone Acetate
- Dosage form
- SUPPOSITORY
- Route
- RECTAL
- Labeler
- Westminster Pharmaceuticals, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2024-11-25
- Substance
- HYDROCORTISONE ACETATE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 3X7931PO74 | HYDROCORTISONE ACETATE | 50-03-3 | HYDROCORTISONE ACETATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 69367-260-12 | 69367026012 | 12 SUPPOSITORY in 1 CARTON (69367-260-12) | 12 suppository | 2024-11-25 | No | No | Historical |