| NDC Code | 0703-0696-01 |
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| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0703-0696-01) > 20 mL in 1 VIAL, MULTI-DOSE |
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| Product NDC | 0703-0696 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Treprostinil |
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| Non-Proprietary Name | Treprostinil |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRAVENOUS; SUBCUTANEOUS |
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| Start Marketing Date | 20190930 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA206648 |
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| Manufacturer | Teva Parenteral Medicines, Inc. |
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| Substance Name | TREPROSTINIL |
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| Strength | 200 |
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| Strength Unit | mg/20mL |
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| Pharmacy Classes | Prostacycline Vasodilator [EPC], Prostaglandins I [CS], Vasodilation [PE] |
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