DEXAMETHASONE SODIUM PHOSPHATE
- Product NDC
- 68071-1866
- 11-digit product format
- 680711866
- Labeler code
- 68071
- Product ID
- 68071-1866_553accf9-f63d-3b80-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DEXAMETHASONE SODIUM PHOSPHATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRAVENOUS; SOFT TISSUE
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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