Hydrocortisone
- Product NDC
- 51672-2018
- 11-digit product format
- 516722018
- Labeler code
- 51672
- Product ID
- 51672-2018_36204f5e-ffd4-0b6c-e063-6394a90a2098
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hydrocortisone
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1989-10-03
- Substance
- HYDROCORTISONE
- Active strength
- 1 g/100g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Hydrocortisone
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HYDROCORTISONE | 1 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | WI4X0X7BPJ |
| Rxcui | 203105 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51672-2018-2 | Hydrocortisone | 28.4 g in 1 TUBE | OINTMENT | 28.4 | | 4 |
| 51672-2018-2 | Hydrocortisone | 1 in 1 CARTON | OINTMENT | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51672-2018 | HYDROCORTISONE OINTMENT [SUN PHARMACEUTICAL INDUSTRIES, INC.] | 4 | Current NDC, Legacy NDC, 2 package rows | 20250529_f7aecfb4-c194-4554-8d05-4e46005e654b.zip |
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 |
|---|
| 51672-2018-2 | 51672201802 | 1 TUBE in 1 CARTON (51672-2018-2) / 28.4 g in 1 TUBE | 1 tube | 1989-10-03 | 0000-00-00 | No | No | Current |