| NDC Code | 51662-1537-3 |
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| Package Description | 25 POUCH in 1 BOX (51662-1537-3) / 1 AMPULE in 1 POUCH (51662-1537-2) / .5 mL in 1 AMPULE |
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| Product NDC | 51662-1537 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Vitamin K1 Phytonadione |
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| Non-Proprietary Name | Vitamin K1, Phytonadione |
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| Dosage Form | INJECTION, EMULSION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
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| Start Marketing Date | 20211101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA087954 |
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| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
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| Substance Name | PHYTONADIONE |
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| Strength | 2 |
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| Strength Unit | mg/mL |
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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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