Dexamethasone
- Product NDC
- 72189-572
- 11-digit product format
- 721890572
- Labeler code
- 72189
- Product ID
- 72189-572_214dea63-d77b-922a-e063-6294a90a967e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_rx
- Application
- ANDA216282
- Marketing category
- ANDA
- Marketing start
- 2024-09-04
- 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 |
|---|
| 72189-572-15 | 72189057215 | 15 TABLET in 1 BOTTLE (72189-572-15) | 15 tablet | 2024-09-04 | No | No | Historical |
| 72189-572-21 | 72189057221 | 21 TABLET in 1 BOTTLE (72189-572-21) | 21 tablet | 2024-09-04 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Dexamethasone | Direct_rx | 2024-09-04 | HUMAN PRESCRIPTION DRUG LABEL | 1 |