Dexamethasone Sodium Phosphate
- Product NDC
- 71872-7239
- 11-digit product format
- 718727239
- Labeler code
- 71872
- Product ID
- 71872-7239_fae6ed45-7b30-0752-e053-6394a90a3c9b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone Sodium Phosphate
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA210967
- Marketing category
- ANDA
- Marketing start
- 2019-06-07
- Substance
- DEXAMETHASONE SODIUM PHOSPHATE
- Active strength
- 100 mg/10mL
- 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 |
|---|
| 71872-7239-1 | 71872723901 | 1 VIAL in 1 BAG (71872-7239-1) / 10 mL in 1 VIAL | 1 vial | 2021-02-15 | No | No | Historical |