Dexamethasone Sodium Phosphate
- Product NDC
- 80425-0261
- 11-digit product format
- 804250261
- Labeler code
- 80425
- Product ID
- 80425-0261_2a9bad62-b2fd-697c-e063-6294a90aa395
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone Sodium Phosphate
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Advanced Rx Pharmacy of Tennessee, LLC
- Application
- ANDA207442
- Marketing category
- ANDA
- Marketing start
- 2023-02-16
- Substance
- DEXAMETHASONE SODIUM PHOSPHATE
- Active strength
- 10 mg/mL
- 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 |
|---|
| AI9376Y64P | DEXAMETHASONE SODIUM PHOSPHATE | 2392-39-4 | DEXAMETHASONE SODIUM PHOSPHATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 80425-0261-1 | 80425026101 | 25 VIAL in 1 CARTON (80425-0261-1) / 1 mL in 1 VIAL | 25 vial | 2023-02-16 | No | No | Historical |