DEXAMETHASONE
- Product NDC
- 72888-239
- 11-digit product format
- 728880239
- Labeler code
- 72888
- Product ID
- 72888-239_99311cd0-f11e-4313-bb8c-eeb09fdcb3f4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DEXAMETHASONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Advagen Pharma Ltd.
- Application
- ANDA218372
- Marketing category
- ANDA
- Marketing start
- 2025-10-15
- Substance
- DEXAMETHASONE
- Active strength
- 2 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 | 2 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7S5I7G3JQL |
| Rxcui | 197577, 197579, 197580, 197581, 197582, 197583, 343033 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72888-239-01 | DEXAMETHASONE | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72888-239-01 | 72888023901 | 100 TABLET in 1 BOTTLE (72888-239-01) | 100 tablet | 2025-10-15 | No | No | Current |