| NDC Code | 0703-1501-02 |
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| Package Description | 5 VIAL, SINGLE-USE in 1 CARTON (0703-1501-02) / 1 mL in 1 VIAL, SINGLE-USE (0703-1501-01) |
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| Product NDC | 0703-1501 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Alprostadil |
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| Non-Proprietary Name | Alprostadil |
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| Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
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| Usage | INTRAVASCULAR |
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| Start Marketing Date | 19990430 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075196 |
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| Manufacturer | Teva Parenteral Medicines, Inc. |
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| Substance Name | ALPROSTADIL |
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| Strength | 500 |
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| Strength Unit | ug/mL |
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| Pharmacy Classes | Genitourinary Arterial Vasodilation [PE], Prostaglandin Analog [EPC], Prostaglandin E1 Agonist [EPC], Prostaglandin Receptor Agonists [MoA], Prostaglandins [CS], Venous Vasodilation [PE] |
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