Dexamethasone
- Product NDC
- 60505-6249
- 11-digit product format
- 605056249
- Labeler code
- 60505
- Product ID
- 60505-6249_4267b6d1-37d3-7ed2-7a89-251185401d0d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Apotex Corp.
- Application
- ANDA217695
- Marketing category
- ANDA
- Marketing start
- 2023-12-05
- Substance
- DEXAMETHASONE
- Active strength
- .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 |
|---|
| 60505-6249-1 | 60505624901 | 100 TABLET in 1 BOTTLE (60505-6249-1) | 100 tablet | 2023-12-05 | No | No | Historical |