Advanced Hydrocortisone
- Product NDC
- 42213-370
- 11-digit product format
- 422130370
- Labeler code
- 42213
- Product ID
- 42213-370_f1b26eb5-bf86-1d24-e053-2a95a90a2f15
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- hydrocortisone
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Ultra Seal Corporation
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2011-04-05
- Marketing end
- 2024-07-01
- Substance
- HYDROCORTISONE
- Active strength
- 10 mg/g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- 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 |
|---|
| 42213-370-09 | 42213037009 | .9 g in 1 PACKET (42213-370-09) | | 2011-04-05 | 0000-00-00 | No | No | Current |
| 42213-370-28 | 42213037028 | 28 g in 1 TUBE (42213-370-28) | 28 g | 2011-04-05 | 0000-00-00 | No | No | Current |
| 42213-370-80 | 42213037080 | 144 PACKET in 1 BOX (42213-370-80) > 1.5 g in 1 PACKET (42213-370-34) | 144 packet | 2011-04-05 | 0000-00-00 | No | No | Current |