Hydrocortisone Butyrate
- Product NDC
- 70512-032
- 11-digit product format
- 705120032
- Labeler code
- 70512
- Product ID
- 70512-032_b8b8c6ab-f51c-036c-e053-2995a90a9e5b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocortisone Butyrate Lotion
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Sola Pharmaceuticals
- Application
- ANDA209556
- Marketing category
- ANDA
- Marketing start
- 2019-02-04
- Marketing end
- 0000-00-00
- Substance
- HYDROCORTISONE BUTYRATE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 70512-032-04 | 70512003204 | 1 TUBE in 1 CARTON (70512-032-04) > 118 mL in 1 TUBE | 1 tube | 2019-02-04 | 0000-00-00 | No | No | Current |