HYDROCORTISONE BUTYRATE
- Product NDC
- 68682-270
- 11-digit product format
- 686820270
- Labeler code
- 68682
- Product ID
- 68682-270_1d2a2e46-dde7-4319-b8c6-a4ac225709a9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HYDROCORTISONE BUTYRATE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Oceanside Pharmaceuticals
- Application
- NDA018514
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2013-07-03
- Marketing end
- 2021-11-30
- Substance
- HYDROCORTISONE BUTYRATE
- Active strength
- 1 mg/g
- 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 |
|---|
| 68682-270-15 | 68682027015 | 1 TUBE in 1 CARTON (68682-270-15) > 15 g in 1 TUBE | 1 tube | 2013-07-03 | 2021-10-31 | No | No | Current |
| 68682-270-45 | 68682027045 | 1 TUBE in 1 CARTON (68682-270-45) > 45 g in 1 TUBE | 1 tube | 2013-07-03 | 2021-11-30 | No | No | Current |