Acyclovir Injection, Powder, Lyophilized, For Solution
Product Images NDC 0143-9657

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This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Acyclovir (NDC 0143-9657). 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.

Product Images & Figures Index

FDA Label Image

Chemical Structure (Acyclovir For Injection Usp 1)

Chemical Structure (Acyclovir For Injection Usp 1)
FDA Label Image

Ndc 0143-9657-01 Acyclovir For Injection, Usp 500 mg/vial For Intravenous Infusion Only Rx Only Single Dose Vial Preparation Of Solution: Inject 10 mL Sterile Water For Injection Into Vial. Shake Vial Until Clear Solution Is Achieved And Use Within 12 Hours. Do Not Use Bacteriostatic Water For Injection Containing Benzyl Alcohol Or Parabens. Dilute To 7 mg/ml Or Lower Prior To Infusion. See Package Insert For Usual Dosage, Reconstitution And Dilution Instructions. Store Between 15º And 25ºc (59º To 77ºf). (Acyclovir For Injection Usp 2)

Ndc 0143-9657-01 Acyclovir For Injection, Usp 500 mg/vial For Intravenous Infusion Only Rx Only Single Dose Vial Preparation Of Solution: Inject 10 mL Sterile Water For Injection Into Vial. Shake Vial Until Clear Solution Is Achieved And Use Within 12 Hours. Do Not Use Bacteriostatic Water For Injection Containing Benzyl Alcohol Or Parabens. Dilute To 7 mg/ml Or Lower Prior To Infusion. See Package Insert For Usual Dosage, Reconstitution And Dilution Instructions. Store Between 15º And 25ºc (59º To 77ºf). (Acyclovir For Injection Usp 2)
FDA Label Image

Ndc 0143-9657-10 Rx Only Acyclovir For Injection, Usp 500 mg/vial For Intravenous Infusion Only 10 Single Dose Vials, 500 mg In Each Vial Each Vial Contains: Acyclovir Sodium Equivalent To 500 mg Of Acyclovir. The Sodium Content Is 49 mg Per Vial. Preparation Of Solution: Inject 10 mL Sterile Water For Injection Into Vial. Shake Vial Until Clear Solution Is Achieved And Use Within 12 Hours. Do Not Use Bacteriostatic Water For Injection Containing Benzyl Alcohol Or Parabens. Dilute To 7 mg/ml Or Lower Prior To Infusion. See Package Insert For Usual Dosage, Reconstitution And Dilution Instructions. Store Between 15º And 25ºc (59º To 77ºf). (Acyclovir For Injection Usp 3)

Ndc 0143-9657-10 Rx Only Acyclovir For Injection, Usp 500 mg/vial For Intravenous Infusion Only 10 Single Dose Vials, 500 mg In Each Vial Each Vial Contains: Acyclovir Sodium Equivalent To 500 mg Of Acyclovir. The Sodium Content Is 49 mg Per Vial. Preparation Of Solution: Inject 10 mL Sterile Water For Injection Into Vial. Shake Vial Until Clear Solution Is Achieved And Use Within 12 Hours. Do Not Use Bacteriostatic Water For Injection Containing Benzyl Alcohol Or Parabens. Dilute To 7 mg/ml Or Lower Prior To Infusion. See Package Insert For Usual Dosage, Reconstitution And Dilution Instructions. Store Between 15º And 25ºc (59º To 77ºf). (Acyclovir For Injection Usp 3)
Acyclovir is a medication for intravenous infusion and it is available in 101 g Single Dose Vials. Each vial contains Acyclovir sodium equivalent to 1 g of acyclovir. Its preparation of solution requires injecting 20 mL of sterile water for injection into the vial and shaking until a clear solution is achieved. This medication should be diluted to 7 mg/mL or lower prior to infusion. The dosage, reconstitution, and dilution instructions are available on the package insert. It is manufactured by HIKMA FARMACEUTICA (PORTUGAL), SA and distributed by Hikma, Berkeley Heights, NJ 07922. Store between 15° and 25°C (59° to 77°F). NDC 0143-9658-10.*
FDA Label Image

Ndc 0143-9658-01 Acyclovir For Injection, Usp 1 G/vial For Intravenous Infusion Only Rx Only Single Dose Vial Preparation Of Solution: Inject 20 mL Sterile Water For Injection Into Vial. Shake Vial Until Clear Solution Is Achieved And Use Within 12 Hours. Do Not Use Bacteriostatic Water For Injection Containing Benzyl Alcohol Or Parabens. Dilute To 7 mg/ml Or Lower Prior To Infusion. See Package Insert For Usual Dosage, Reconstitution And Dilution Instructions. Store Between 15º And 25ºc (59º To 77ºf). (Acyclovir For Injection Usp 4)

Ndc 0143-9658-01 Acyclovir For Injection, Usp 1 G/vial For Intravenous Infusion Only Rx Only Single Dose Vial Preparation Of Solution: Inject 20 mL Sterile Water For Injection Into Vial. Shake Vial Until Clear Solution Is Achieved And Use Within 12 Hours. Do Not Use Bacteriostatic Water For Injection Containing Benzyl Alcohol Or Parabens. Dilute To 7 mg/ml Or Lower Prior To Infusion. See Package Insert For Usual Dosage, Reconstitution And Dilution Instructions. Store Between 15º And 25ºc (59º To 77ºf). (Acyclovir For Injection Usp 4)
Acyclovir is a medication that is administered through intravenous infusion. It comes in a single-dose vial that contains 500mg per vial. To prepare the solution, it is necessary to inject 10mL of sterile water into the vial, shake it, and use it within 12 hours. It is important to not use bacteriostatic water for injection that contains benzyl alcohol or parabens. Before infusion, it must be diluted to 7mg/m or lower. It is advisable to check the package insert for information on dosage, reconstitution, and dilution. The medication must be stored between 15° and 25°C.*
FDA Label Image

Ndc 0143-9658-10 Rx Only Acyclovir For Injection, Usp 1 G/vial For Intravenous Infusion Only 10 Single Dose Vials, 1 G In Each Vial Each Vial Contains: Acyclovir Sodium Equivalent To 1 G Of Acyclovir. The Sodium Content Is 98 mg Per Vial. Preparation Of Solution: Inject 20 mL Sterile Water For Injection Into Vial. Shake Vial Until Clear Solution Is Achieved And Use Within 12 Hours. Do Not Use Bacteriostatic Water For Injection Containing Benzyl Alcohol Or Parabens. Dilute To 7 mg/ml Or Lower Prior To Infusion. See Package Insert For Usual Dosage, Reconstitution And Dilution Instructions. Store Between 15º And 25ºc (59º To 77ºf). (Acyclovir For Injection Usp 5)

Ndc 0143-9658-10 Rx Only Acyclovir For Injection, Usp 1 G/vial For Intravenous Infusion Only 10 Single Dose Vials, 1 G In Each Vial Each Vial Contains: Acyclovir Sodium Equivalent To 1 G Of Acyclovir. The Sodium Content Is 98 mg Per Vial. Preparation Of Solution: Inject 20 mL Sterile Water For Injection Into Vial. Shake Vial Until Clear Solution Is Achieved And Use Within 12 Hours. Do Not Use Bacteriostatic Water For Injection Containing Benzyl Alcohol Or Parabens. Dilute To 7 mg/ml Or Lower Prior To Infusion. See Package Insert For Usual Dosage, Reconstitution And Dilution Instructions. Store Between 15º And 25ºc (59º To 77ºf). (Acyclovir For Injection Usp 5)
This appears to be a description of a medication product, specifically a solution containing acyloit sodium. The solution comes in a vial and has instructions for reconstitution and dilution before intravenous infusion. It is important to note that the solution should not be mixed with certain other substances. It should be stored at a temperature between 15°C and 25°C. The medication is manufactured by Hikma Farmaceutica in Portugal.*
FDA Label Image

Acyclovir For Injection Usp 6

Acyclovir For Injection Usp 6
This is a product identification code containing the GTIN (Global Trade Item Number), serial number (SN), expiration date (EXP), and lot number (LOT). The GTIN is a unique product identifier used globally. The SN is a unique identification number given to a specific item. The EXP indicates when the item is expected to expire, with MMM representing the month and YYYY representing the year. The LOT is a batch number used to identify groups of products that were manufactured together.*

* 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.