Dexamethasone Sodium Phosphate
- Product NDC
- 52584-421
- 11-digit product format
- 525840421
- Labeler code
- 52584
- Product ID
- 52584-421_4c1a6269-b693-454e-8554-e8fad49e2444
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone Sodium Phosphate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRAVENOUS; SOFT TISSUE
- Labeler
- General Injectables and Vaccines, Inc
- Application
- ANDA040803
- Marketing category
- ANDA
- Marketing start
- 2015-08-21
- Marketing end
- 2022-06-30
- Substance
- DEXAMETHASONE SODIUM PHOSPHATE
- Active strength
- 4 mg/mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-421-00 | 52584042100 | 1 VIAL, MULTI-DOSE in 1 BAG (52584-421-00) > 30 mL in 1 VIAL, MULTI-DOSE | 2015-08-21 | 0000-00-00 | No | No | Current |