| NDC Code | 70095-154-02 |
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| Package Description | 10 CARTON in 1 CARTON (70095-154-02) / 1 BLISTER PACK in 1 CARTON (70095-154-01) / 1 SYRINGE in 1 BLISTER PACK / .5 mL in 1 SYRINGE |
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| Product NDC | 70095-154 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Phytonadione |
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| Non-Proprietary Name | Phytonadione |
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| Dosage Form | INJECTION, EMULSION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
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| Start Marketing Date | 20260610 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA216298 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | PHYTONADIONE |
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| Strength | 1 |
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| Strength Unit | mg/.5mL |
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| Pharmacy Classes | Increased Prothrombin Activity [PE], Reversed Anticoagulation Activity [PE], Vitamin K [CS], Vitamin K [EPC], Warfarin Reversal Agent [EPC] |
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