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DEXAMETHASONE SODIUM PHOSPHATE
DEXAMETHASONE SODIUM PHOSPHATE - 0069-4543-02 - (DEXAMETHASONE SODIUM PHOSPHATE)
Drug Information of DEXAMETHASONE SODIUM PHOSPHATE
| Product NDC: | 0069-4543 |
| Proprietary Name: | DEXAMETHASONE SODIUM PHOSPHATE |
| Non Proprietary Name: | DEXAMETHASONE SODIUM PHOSPHATE |
| Active Ingredient(s): | 4 mg/mL & nbsp; DEXAMETHASONE SODIUM PHOSPHATE |
| Administration Route(s): | INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRAVENOUS; SOFT TISSUE |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DEXAMETHASONE SODIUM PHOSPHATE
| Product NDC: | 0069-4543 |
| Labeler Name: | Pfizer Laboratories Div Pfizer Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040803 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110511 |
Package Information of DEXAMETHASONE SODIUM PHOSPHATE
| Package NDC: | 0069-4543-02 |
| Package Description: | 25 VIAL in 1 CARTON (0069-4543-02) > 5 mL in 1 VIAL (0069-4543-01) |
NDC Information of DEXAMETHASONE SODIUM PHOSPHATE
| NDC Code | 0069-4543-02 |
| Proprietary Name | DEXAMETHASONE SODIUM PHOSPHATE |
| Package Description | 25 VIAL in 1 CARTON (0069-4543-02) > 5 mL in 1 VIAL (0069-4543-01) |
| Product NDC | 0069-4543 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DEXAMETHASONE SODIUM PHOSPHATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRAVENOUS; SOFT TISSUE |
| Start Marketing Date | 20110511 |
| Marketing Category Name | ANDA |
| Labeler Name | Pfizer Laboratories Div Pfizer Inc |
| Substance Name | DEXAMETHASONE SODIUM PHOSPHATE |
| Strength Number | 4 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
