Dexamethasone Sodium Phosphate
- Product NDC
- 71872-7347
- 11-digit product format
- 718727347
- Labeler code
- 71872
- Product ID
- 71872-7347_41eb3ab8-1602-c9c4-e063-6294a90a4cd0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone Sodium Phosphate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRAVENOUS; SOFT TISSUE
- Labeler
- Medical Purchasing Solutions, LLC.
- Application
- ANDA215654
- Marketing category
- ANDA
- Marketing start
- 2024-12-01
- Substance
- DEXAMETHASONE SODIUM PHOSPHATE
- Active strength
- 4 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 |
|---|
| 71872-7347-1 | 71872734701 | 1 VIAL in 1 BAG (71872-7347-1) / 5 mL in 1 VIAL | 1 vial | 2025-04-21 | No | No | Historical |