Vitamin K1 - Phytonadione Injection, Emulsion
Product Images NDC 51662-1536

VITAMIN K1 INJ. PHYTONADIONE INJECTABLE is a medication that comes in an emulsion form, having a concentration of 10mg/mL and packed in a 1mL AMP. It has an NDC number of 51662-1536-2 and an expiration date of 2030-01-01. To maintain effectiveness, it needs protection from light, kept in the tray until use, and stored at a temperature of 20-25° (68 to 77°F). For intramuscular, subcutaneous, or intravenous use with caution, it may have contained hydrochloric acid for pH regulation with the dose specified in the insert. RX ONLY; manufactured by HF Acquisition Co., LLC, Mukilteo, WA 98275.*

This text is a warning about the use of phytonadione through INTRAVENOUS and INTRAMUSCULAR administration. Severe reactions, even fatal ones, have been reported after injections, resembling hypersensitivity and anaphylaxis, involving shock and cardiac and/or respiratory arrest. The subcutaneous route should be used when possible, and the other routes should be restricted to situations where it is not feasible and the serious risk involved is justified.*

This text provides dosage guidelines for Vitamin K injection (Phytonadione Injectable Emulsion, USP) for different age groups and conditions, with details on the dosage range for each case. For newborns with Hemorrhagic Disease of the Newborn, the recommended dosage is 0.5 to 1 mg IM within the first hour of birth. For adults, the initial dosage for Anticoagulant-Induced Prothrombin Deficiency is 2.5mg to 10 mg or up to 25 mg, and for Hypoprothrombinemia caused by other factors, it is 2.5 mg to 25 mg, with doses rarely up to 50 mg.*

Vitamin K1 Injection is a medication available in 1mg/0.5 mL and 10 mg/mL formulations, packaged in bundles of 5 clamshell packs each containing single-dose ampoules. It has to be stored between 20 to 25°C (68 to 77°F) and protected from light until use. The medication is distributed by Hospira, Inc., Lake Forest, IL 60045 USA.*

This is a description of a Vitamin K injection contained in a single-dose ampoule. The ampoules are intended for prescription use only and must be protected from light by storing in the tray until use. The injection is suitable for Intramuscular, Subcutaneous, or Intravenous (with caution). The injection contains phytonadione 10 mg, polyoxyethylated fatty acid derivative 70 mg, dextrose, hydrous 37.5 mg, and benzyl alcohol 9mg added as preservative. The injection may contain hydrochloric acid for pH adjustment with a pH range of 6.3 (5.0 to 7.0). The usual dosage should be seen in the insert. The injection should be stored at a temperature range of 20°C to 25°C (68°F to 77°F). The distribution company is Hospira, Inc., Lake Forest, 1L 60045 USA.*

This is a description of a vitamin K injection. The injection comes in an emulsion form and has a concentration of 10 mg/mL. The product contains less than 110 meg/L of aluminum and should be protected from light. The product code is NDC0409-9158-37 and the prescription is required for purchase. There is also a lot/exp area with the letters SVP.*