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Phytonadione
Phytonadione - 52584-140-00 - (Phytonadione)
Drug Information of Phytonadione
| Product NDC: | 52584-140 |
| Proprietary Name: | Phytonadione |
| Non Proprietary Name: | Phytonadione |
| Active Ingredient(s): | 1 mg/.5mL & nbsp; Phytonadione |
| Administration Route(s): | INTRAMUSCULAR; PARENTERAL; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phytonadione
| Product NDC: | 52584-140 |
| Labeler Name: | General Injectables & Vaccine, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA083722 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100401 |
Package Information of Phytonadione
| Package NDC: | 52584-140-00 |
| Package Description: | 1 CARTON in 1 BAG (52584-140-00) > 1 SYRINGE in 1 CARTON > .5 mL in 1 SYRINGE |
NDC Information of Phytonadione
| NDC Code | 52584-140-00 |
| Proprietary Name | Phytonadione |
| Package Description | 1 CARTON in 1 BAG (52584-140-00) > 1 SYRINGE in 1 CARTON > .5 mL in 1 SYRINGE |
| Product NDC | 52584-140 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phytonadione |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; PARENTERAL; SUBCUTANEOUS |
| Start Marketing Date | 20100401 |
| Marketing Category Name | ANDA |
| Labeler Name | General Injectables & Vaccine, Inc |
| Substance Name | PHYTONADIONE |
| Strength Number | 1 |
| Strength Unit | mg/.5mL |
| Pharmaceutical Classes | Increased Prothrombin Activity [PE],Reversed Anticoagulation Activity [PE],Vitamin K [Chemical/Ingredient],Vitamin K [EPC],Warfarin Reversal Agent [EPC] |
