Haloperidol Decanoate Injection
Product Images NDC 70710-1461

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Haloperidol Decanoate (NDC 70710-1461). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus 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.

FDA Label Image

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FDA Label Image

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This is a description of Haloperidol injection. It comes in a 1 mL single-dose vial and each mL contains 50 mg of Haloperidol. It is meant for intramuscular use only and should be stored between 20°C to 25°C (68°F to 77°F). The product is distributed by Zydus Pharmaceuticals (USA) Inc. and the lot number is not provided.*

FDA Label Image

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This is a Haloperidol Decanoate Injection, used only for intramuscular injection. Each mL contains 50 mg haloperidol as 70.52 mg haloperidol decanoate in a sesame oil vehicle and should not be refrigerated or frozen but protected from light. The usual dosage information can be found in the package insert. The product is distributed by Zydus Pharmaceuticals (USA) Inc.*

FDA Label Image

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This text describes a medication labeled as "Haloperidol Decanoate Injection". It is a single-dose vial containing 1 mL of the injection that is intended to be administered intramuscularly only. Each mL of the injection contains 100mg of Haloperidol. The medication should not be refrigerated or frozen and must be protected from light. The manufacturer is Zydus Pharmaceuticals (USA) Inc, and the product was made in India. The NDC number of the medication is 70710-14631.*

FDA Label Image

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Haloperidol Decanoate is an injectable medication used for intramuscular use only. It contains 100 mg of haloperidol per mL as 141.04 mg of haloperidol decanoate in sesame oil. It also contains benzyl alcohol as a preservative at a concentration of 1.2 %. The medication should be stored at 20°C to 25°C and protected from light. It is recommended not to refrigerate or freeze the medication. The usual dosage information is provided in the package insert. It is a multiple-dose vial and should be retained in its carton until use. This product is manufactured in Italy and distributed by Zydus Pharmaceuticals USA Inc. This medication is available by prescription only.*

FDA Label Image

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This is a product label for Haloperidol Decanoate Injection, used for intramuscular use only. The concentration is 0mg/mL.*

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FDA Label Image

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This is an informational text about Haloperidol Decanoate Injection, which contains 250 mg/5 ml, and comes in a bundle supply. The substrate used is a 300 GSM FBB board with a varnish, and the packaging includes a carton with a built-in partition. No further information is available.*

FDA Label Image

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Haloperidol Decanoate Injection is a medication used only for intramuscular use with a prescribed dosage. It is manufactured by Ui Pharmaceuticals and distributed by Zydus Pharmaceuticals (USA) Inc. The medication comes in a 5x5 mL multiple-dose vial, and the usual dosage information can be found in the package insert. The medication contains 250 mg/5 mL (50 mg/mL) of Haloperidol Decanoate. Protect from light and store at room temperature. The box contains a warning to retain the original packaging and indicates that the container was not made in a natural nitrate environment.*

FDA Label Image

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FDA Label Image

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FDA Label Image

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Haloperidol Decanoate Injection is an intramuscular medication used for the treatment of certain mental/mood disorders. The injection contains 500mg of Haloperidol Decanoate per 5mL vial. This medication is only for use on patients under medical supervision. The package includes a FBB board with an aqua varnish coating, which should be stored with a built-in partition.*

FDA Label Image

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* 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.