Vitamin K1 Injection, Emulsion
Product Images NDC 0409-9158

This is a description of a prescription-only medication called Phytonadione Inj ectable Emulsion. It is a Vitamin K injection that comes in a single-dose ampule of 1mg/0.5 mL concentration intended for neonatal use, containing no more than 100 mcg/L of aluminum. The medication should be protected from light and is distributed by Hospira, Inc. The text also includes a reference number and date code.*

This is a description of a medication in the form of a single-dose ampule containing 1mg/0.5mL of Phytonadione Injectable Emulsion, USP - Vitamin K1 Injection. It is intended for neonatal concentration and can be administered intramuscularly, subcutaneously, or intravenously with caution. The medication should be protected from light, and the ampules should be kept in the tray until the time of use. The medication contains phytonadione 2 mg, polyoxyethylated fatty acid derivative 70 mg, dextrose, hydrous 37.5 mg, and benzyl alcohol 9 mg as a preservative. However, it may contain hydrochloric acid for pH adjustment. The usual dosage should be checked from the insert, and it should be stored at a temperature of 20 to 25°C. The medication is distributed by Hospira, Inc., in Lake Forest, IL 60045 USA, and its reference number is RL-7129.*

This is a description of a single-dose ampule of injectable Vitamin K (Phytonadione) emulsion, with a strength of 10mg/mL. It contains no more than 110 mcg of aluminum and needs to be protected from light. This product is distributed by Hospira, Inc. and is intended for use with a prescription. The rest of the text contains code information that is not relevant to the product description.*

This is a description of a Vitamin K1 injectable emulsion, USP, with a concentration of 10 mg/mL, contained in a 1 mL single-dose ampule. The medication is to be protected from light and kept in the tray until use. It can be administered intramuscularly, subcutaneously, or intravenously with caution. The injection includes phytonadione 10 mg, polyoxyethylated fatty acid derivative 70 mg, dextrose hydrous 37.5 mg, and benzyl alcohol 9 mg as a preservative. The solution may contain hydrochloric acid for PH adjustment. The usual dosage is provided in the insert, and the medication should be stored at 20 to 25°C (68-77°F). The medication is distributed by Hospira, Inc. The text also includes other relevant details such as the NDC code, manufacturer location, and expiration area.*

This is a single-dose Ampul containing phytonadione injectable emulsion USP used for Intramuscular, Subcutaneous, or Intravenous administration. It is stored in a tray and protected from light. Each 1 mL of the solution contains phytonadione 10mg, polyoxyethylated fatty acid derivative 70mg, dextrose hydrous 37.5mg, and benzyl alcohol 9mg added as preservative. It may contain hydrochloric acid for pH adjustment. The usual dosage instructions are on the insert. It is distributed by Hospira, Inc. and is trademarked as Novaplus. The solution should be stored at 20 to 25°C.*