Dexamethasone Sodium Phosphate
- Product NDC
- 68071-4580
- 11-digit product format
- 680714580
- Labeler code
- 68071
- Product ID
- 68071-4580_76e273f4-8783-3fe3-e053-2a91aa0ad4cf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DEXAMETHASONE SODIUM PHOSPHATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA084916
- Marketing category
- ANDA
- Marketing start
- 2000-09-07
- 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