Dexamethasone Sodium Phosphate
- Product NDC
- 70518-3019
- 11-digit product format
- 705183019
- Labeler code
- 70518
- Product ID
- 70518-3019_e5333c2e-03d1-23bb-e053-2a95a90ade22
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone Sodium Phosphate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRAVENOUS; SOFT TISSUE
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040803
- Marketing category
- ANDA
- Marketing start
- 2021-02-08
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3019-0 | 70518301900 | 25 VIAL in 1 CARTON (70518-3019-0) > 1 mL in 1 VIAL (70518-3019-1) | 25 vial | 2021-02-08 | 0000-00-00 | No | No | Current |