DEXAMETHASONE SODIUM PHOSPHATE
- Product NDC
- 55154-8338
- 11-digit product format
- 551548338
- Labeler code
- 55154
- Product ID
- 55154-8338_d847d1fa-1015-4fa6-aefd-99646b68a2b5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DEXAMETHASONE SODIUM PHOSPHATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRAVENOUS; SOFT TISSUE
- Labeler
- Cardinal Health
- Application
- ANDA206781
- Marketing category
- ANDA
- Marketing start
- 2015-12-01
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- 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 |
|---|
| 55154-8338-5 | 55154833805 | 5 VIAL, SINGLE-DOSE in 1 BAG (55154-8338-5) > 1 mL in 1 VIAL, SINGLE-DOSE | 2015-12-01 | 0000-00-00 | No | No | Current |