Cefazolin Injection, Powder, For Solution
Product Images NDC 0143-9924

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Cefazolin (NDC 0143-9924). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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Chemical Structure (Cefazolin For Injection 1)

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Ndc 0143-9923-90 Cefazolin For Injection, Usp 500 mg*/vial For Iv Or Im Use Rx Only * Each Vial Contains Sterile Cefazolin Sodium Equivalent To 500 mg Cefazolin. The Sodium Content Is 24 mg. Usual Adult Dosage: 250 mg To 1 Gram Every 6 To 8 Hours. For More Information See Package Insert. For Im Administration: Add 2.0 mL Of Sterile Water For Injection. Shake Well To Dissolve. Withdraw Entire Contents. Provides An Approximate Volume Of 2.2 mL (225 mg/ml). For Iv Administration: See Package Insert. Reconstituted Solution Is Stable For 24 Hours At Room Temperature Or For 10 Days Under Refrigeration (5ºc Or 41ºf). Reconstituted Solutions May Range In Color From Pale Yellow To Yellow Without A Change In Potency. Store At 20º To 25ºc (68º To 77ºf) [see Usp Controlled Room Temperature]. Protect From Light. (Cefazolin For Injection 2)

Cefazolin is a medication used for intravenous or intramuscular use. The medication is available in vials containing sterilized cefazolin sodium equivalent to 500mg of cefazolin with a sodium content of 24mg. The usual adult dosage is 250mg to 1 gram every 6 to 8 hours. For intramuscular administration, 20 ml of Sterile Water for Injection should be added and shaken well to dissolve, and the entire contents should be withdrawn. The reconstituted solution is stable for 24 hours at room temperature or up to 10 days under refrigeration at 4 to 17 degrees Celsius. Reconstituted solutions may range in color from pale yellow to yellow without a change in potency. Store at 20°C to 25°C. This medication is distributed by Hikma in Berkeley Heights, NJ. For more information, see the package insert.*

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Ndc 0143-9924-90 Cefazolin For Injection, Usp 1 Gram*/vial For Iv Or Im Use Rx Only * Each Vial Contains Sterile Cefazolin Sodium Equivalent To 1 Gram Cefazolin. The Sodium Content Is 48 mg. Usual Adult Dosage: 250 mg To 1 Gram Every 6 To 8 Hours. For More Information See Package Insert. For Im Administration: Add 2.5 mL Of Sterile Water For Injection. Shake Well To Dissolve. Withdraw Entire Contents. Provides An Approximate Volume Of 3.0 mL (330 mg/ml). For Iv Administration: See Package Insert. Reconstituted Solution Is Stable For 24 Hours At Room Temperature Or For 10 Days Under Refrigeration (5ºc Or 41ºf). Reconstituted Solutions May Range In Color From Pale Yellow To Yellow Without A Change In Potency. Store At 20º To 25ºc (68º To 77ºf) [see Usp Controlled Room Temperature]. Protect From Light. (Cefazolin For Injection 3)

Cefazolin is a medication available in vial form for injection in either intravenous or intramuscular administration. Each vial contains 500 mg of the medication, and a package of vials should be used within 24 hours of opening. The medication is sold by Hikma Pharmaceuticals under the NDC code 0143-9923-30 for prescription purposes only.*

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Cefazolin For Injection 4

Cefazolin is an antibiotic medication that comes in the form of a powder for intravenous or intramuscular use. Each vial contains 1 gram of Cefazolin sodium that is equivalent to 1 gram of Cefazolin, with a sodium content of 48mg. The usual adult dosage involves administering 250mg to 1 gram every 6-8 hours. For administering intramuscularly, one must add 25ml of sterile water for injection and shake it well to dissolve. Withdraw the entire contents of the vial to get an approximate volume of 30mL. The information on reconstituted solutions and storage instructions are available in the package insert. The manufacturer of Cefazolin is HIKMA FARMACEUTICA (PORTUGAL), S.A, and it is distributed in Berkeley Heights, NJ.*

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Cefazolin For Injection 5

Cefazolin is a type of medication used for intravenous or intramuscular use. It comes packaged in 25 vials each containing 1 gram of Cefazolin for Injection, USP. It is only available through a prescription from a physician. Proper administration of the medication is required and as such, instructions on how to administer for both Intramuscular and Intravenous use of the medication are provided. The medication should be stored at room temperature. Additional information can be obtained from healthcare providers. The manufacturer of this particular medication is Hikma Farmaceltica from Portugal.*

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Cefazolin For Injection 6

This is a label for a Pharmacy Bulk Package of Cefazolin for Injection, meant for intravenous use (IV) only. The bulk package contains 10 grams of the medication and is not intended to be dispensed as a unit. The label warns that the package is not for direct infusion and should only be used for preparing a single dose or for compounding. The manufacturer, Hikma Pharmaceutica, is also listed on the label.*

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Cefazolin For Injection 7

Cefazolin for Injection, USP is available in a Pharmacy Bulk Package containing 10 grams of the medication. This medication is intended for intravenous use only and should not be infused directly. The package includes 10x10 g vials and is to be dispensed by a pharmacy. NDC number 0143-9983-03 refers to this medication. The manufacturer is Hikma Pharmaceuticals located in Portugal. The unreadable text at the bottom of the page may contain additional information but due to poor quality caused by it is not legible.*

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Cefazolin For Injection 8

This is a product identification label containing the Global Trade Item Number (GTIN), serial number (SN), expiration date (EXP) and lot number (LOT). The specific product information cannot be determined without additional context.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.