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Dexamethasone Sodium Phosphate
Dexamethasone Sodium Phosphate - 63323-506-01 - (DEXAMETHASONE SODIUM PHOSPHATE)
Drug Information of Dexamethasone Sodium Phosphate
| Product NDC: | 63323-506 |
| Proprietary Name: | Dexamethasone Sodium Phosphate |
| Non Proprietary Name: | DEXAMETHASONE SODIUM PHOSPHATE |
| Active Ingredient(s): | 10 mg/mL & nbsp; DEXAMETHASONE SODIUM PHOSPHATE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dexamethasone Sodium Phosphate
| Product NDC: | 63323-506 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040491 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030529 |
Package Information of Dexamethasone Sodium Phosphate
| Package NDC: | 63323-506-01 |
| Package Description: | 25 VIAL in 1 TRAY (63323-506-01) > 1 mL in 1 VIAL |
NDC Information of Dexamethasone Sodium Phosphate
| NDC Code | 63323-506-01 |
| Proprietary Name | Dexamethasone Sodium Phosphate |
| Package Description | 25 VIAL in 1 TRAY (63323-506-01) > 1 mL in 1 VIAL |
| Product NDC | 63323-506 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DEXAMETHASONE SODIUM PHOSPHATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20030529 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | DEXAMETHASONE SODIUM PHOSPHATE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
