Dexamethasone
- Product NDC
- 72189-468
- 11-digit product format
- 721890468
- Labeler code
- 72189
- Product ID
- 72189-468_2c4deb3e-a1c6-75c0-e063-6394a90a9cb7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA215604
- Marketing category
- ANDA
- Marketing start
- 2023-05-04
- Substance
- DEXAMETHASONE
- Active strength
- 1.5 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 7S5I7G3JQL | DEXAMETHASONE | 50-02-2 | DEXAMETHASONE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-468-15 | 72189046815 | 15 TABLET in 1 BOTTLE (72189-468-15) | 15 tablet | 2023-05-04 | No | No | Historical |
| 72189-468-21 | 72189046821 | 21 TABLET in 1 BOTTLE (72189-468-21) | 21 tablet | 2023-05-04 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Dexamethasone | Direct_Rx | 2025-01-22 | HUMAN PRESCRIPTION DRUG LABEL | 2 |