Hydrocortisone Butyrate
- Product NDC
- 68682-273
- 11-digit product format
- 686820273
- Labeler code
- 68682
- Product ID
- 68682-273_39b5a351-220e-4e22-ac36-ee01e5dedf11
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrocortisone butyrate
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Oceanside Pharmaceuticals
- Application
- NDA019116
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1987-02-25
- Marketing end
- 2021-05-31
- Substance
- HYDROCORTISONE BUTYRATE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68682-273-61 | 68682027361 | 1 BOTTLE in 1 CARTON (68682-273-61) > 60 mL in 1 BOTTLE | 1 bottle | 1987-02-25 | 2021-05-31 | No | No | Current |