Dexamethasone
- Product NDC
- 68071-3603
- 11-digit product format
- 680713603
- Labeler code
- 68071
- Product ID
- 68071-3603_17f5723c-228d-3e4a-e063-6394a90a3388
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA215604
- Marketing category
- ANDA
- Marketing start
- 2022-08-08
- 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
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 |
|---|
| 68071-3603-8 | 68071360308 | 8 TABLET in 1 BOTTLE (68071-3603-8) | 8 tablet | 2024-05-08 | No | No | Historical |