| NDC Code | 0069-0192-02 |
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| Package Description | 25 VIAL in 1 CARTON (0069-0192-02) > 30 mL in 1 VIAL (0069-0192-01) |
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| Product NDC | 0069-0192 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dexamethasone Sodium Phosphate |
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| Non-Proprietary Name | Dexamethasone Sodium Phosphate |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRAVENOUS; SOFT TISSUE |
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| Start Marketing Date | 20110511 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040803 |
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| Manufacturer | Pfizer Laboratories Div Pfizer Inc |
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| Substance Name | DEXAMETHASONE SODIUM PHOSPHATE |
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| Strength | 4 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
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