Hydrocortisone
- Product NDC
- 50382-024
- 11-digit product format
- 503820024
- Labeler code
- 50382
- Product ID
- 50382-024_ee8665e4-eb23-2f51-e053-2995a90a8770
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hydrocortisone
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Galentic Pharma (India) Private Limited
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2013-08-07
- Marketing end
- 0000-00-00
- Substance
- HYDROCORTISONE
- Active strength
- 10 mg/g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50382-024-11 | 50382002411 | 144 PACKET in 1 CARTON (50382-024-11) > .9 g in 1 PACKET | 144 packet | 2016-04-27 | 0000-00-00 | No | No | Current |
| 50382-024-13 | 50382002413 | 1 TUBE in 1 CARTON (50382-024-13) > 28 g in 1 TUBE | 1 tube | 2013-08-07 | 0000-00-00 | No | No | Current |