DEXAMETHASONE
- Product NDC
- 72189-254
- 11-digit product format
- 721890254
- Labeler code
- 72189
- Product ID
- 72189-254_2c28e5cd-de70-cb2d-e063-6394a90ab7f2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DEXAMETHASONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct Rx
- Application
- ANDA084612
- Marketing category
- ANDA
- Marketing start
- 2021-09-20
- Substance
- DEXAMETHASONE
- Active strength
- 4 mg/1
- 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
- DEXAMETHASONE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DEXAMETHASONE | 4 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7S5I7G3JQL |
| Rxcui | 197582 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-254-10 | DEXAMETHASONE | 10 in 1 BOTTLE | TABLET | 10 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-254 | DEXAMETHASONE TABLET [DIRECT RX] | 2 | Current NDC, Legacy NDC, 1 package rows | 20250121_cc7140de-a205-f675-e053-2995a90ac22b.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 |
|---|
| 72189-254-10 | 72189025410 | 10 TABLET in 1 BOTTLE (72189-254-10) | 10 tablet | 2021-09-20 | 0000-00-00 | No | No | Current |