HYDROCORTISONE
- Product NDC
- 68151-2269
- 11-digit product format
- 681512269
- Labeler code
- 68151
- Product ID
- 68151-2269_b0f9b7ea-bac2-427d-92fa-4ccf1b149332
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrocortisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA040646
- Marketing category
- ANDA
- Marketing start
- 2007-03-30
- Marketing end
- 0000-00-00
- Substance
- HYDROCORTISONE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 68151-2269-1 | HYDROCORTISONE | 1 in 1 PACKAGE | TABLET | 1 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-2269 | HYDROCORTISONE TABLET [CARILION MATERIALS MANAGEMENT] | 2 | Legacy NDC, 1 package rows | 20140707_d4d2912e-d1e8-4b40-af88-59c87fa12318.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-2269-1 | 68151226901 | 1 in 1 PACKAGE | Historical |