Hydrocortisone
- Product NDC
- 50436-2143
- 11-digit product format
- 504362143
- Labeler code
- 50436
- Product ID
- 50436-2143_01d045b8-1007-43cf-88cc-7b137828faf6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocortisone
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Unit Dose Services
- Application
- ANDA089414
- Marketing category
- ANDA
- Marketing start
- 1986-12-16
- Marketing end
- 0000-00-00
- Substance
- HYDROCORTISONE
- Active strength
- 25 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-2143-1 | Hydrocortisone | 30 g in 1 TUBE | CREAM | 30 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-2143 | HYDROCORTISONE CREAM [UNIT DOSE SERVICES] | 6 | Legacy NDC, 1 package rows | 20170722_0e606cee-da75-416d-81a3-b90faf9b8528.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 50436-2143-1 | 50436214301 | 30 g in 1 TUBE | 30 g | Historical |