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Vitamin K1
Vitamin K1 - 0409-9157-01 - (PHYTONADIONE)
Drug Information of Vitamin K1
| Product NDC: | 0409-9157 |
| Proprietary Name: | Vitamin K1 |
| Non Proprietary Name: | PHYTONADIONE |
| Active Ingredient(s): | 2 mg/mL & nbsp; PHYTONADIONE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vitamin K1
| Product NDC: | 0409-9157 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087954 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110824 |
Package Information of Vitamin K1
| Package NDC: | 0409-9157-01 |
| Package Description: | 5 TRAY in 1 CONTAINER (0409-9157-01) > 5 AMPULE in 1 TRAY > .5 mL in 1 AMPULE |
NDC Information of Vitamin K1
| NDC Code | 0409-9157-01 |
| Proprietary Name | Vitamin K1 |
| Package Description | 5 TRAY in 1 CONTAINER (0409-9157-01) > 5 AMPULE in 1 TRAY > .5 mL in 1 AMPULE |
| Product NDC | 0409-9157 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PHYTONADIONE |
| Dosage Form Name | INJECTION, EMULSION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 20110824 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | PHYTONADIONE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Increased Prothrombin Activity [PE],Reversed Anticoagulation Activity [PE],Vitamin K [Chemical/Ingredient],Vitamin K [EPC],Warfarin Reversal Agent [EPC] |
