Dexamethasone Sodium Phosphate
- Product NDC
- 76420-185
- 11-digit product format
- 764200185
- Labeler code
- 76420
- Product ID
- 76420-185_b4ea9bea-3f7b-4dc9-e053-2a95a90ae557
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone Sodium Phosphate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRAVENOUS; SOFT TISSUE
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA040803
- Marketing category
- ANDA
- Marketing start
- 2011-05-11
- 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 |
|---|
| 76420-185-01 | 76420018501 | 1 mL in 1 VIAL (76420-185-01) | 1 ml | 2020-11-21 | No | No | Historical |