Product NDC: | 0548-1240 |
Proprietary Name: | Phytonadione |
Non Proprietary Name: | Phytonadione |
Active Ingredient(s): | 1 mg/.5mL & nbsp; Phytonadione |
Administration Route(s): | PARENTERAL |
Dosage Form(s): | INJECTION, EMULSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0548-1240 |
Labeler Name: | Amphastar Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA083722 |
Marketing Category: | ANDA |
Start Marketing Date: | 20030418 |
Package NDC: | 0548-1240-00 |
Package Description: | 25 SYRINGE in 1 CARTON (0548-1240-00) > .5 mL in 1 SYRINGE |
NDC Code | 0548-1240-00 |
Proprietary Name | Phytonadione |
Package Description | 25 SYRINGE in 1 CARTON (0548-1240-00) > .5 mL in 1 SYRINGE |
Product NDC | 0548-1240 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Phytonadione |
Dosage Form Name | INJECTION, EMULSION |
Route Name | PARENTERAL |
Start Marketing Date | 20030418 |
Marketing Category Name | ANDA |
Labeler Name | Amphastar Pharmaceuticals, 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] |