| NDC Code | 70095-026-02 |
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| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (70095-026-02) / 1 mL in 1 VIAL, SINGLE-DOSE (70095-026-01) |
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| Product NDC | 70095-026 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Desmopressin Acetate |
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| Non-Proprietary Name | Desmopressin Acetate |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRAVENOUS; SUBCUTANEOUS |
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| Start Marketing Date | 20230403 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA216922 |
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| Manufacturer | Sun Pharmaceutical Industries Limited |
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| Substance Name | DESMOPRESSIN ACETATE |
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| Strength | 4 |
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| Strength Unit | ug/mL |
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| Pharmacy Classes | Factor VIII Activator [EPC], Increased Coagulation Factor VIII Activity [PE], Increased Coagulation Factor VIII Concentration [PE], Vasopressin Analog [EPC], Vasopressins [CS] |
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