Haloperidol Decanoate Injection
Product Images NDC 70069-382

Product Visual Gallery

This gallery contains 23 technical images submitted to the FDA as part of the official labeling for Haloperidol Decanoate (NDC 70069-382). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, Llc, 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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Chemical structure of haloperidol decanoate, depicting its molecular composition with fluorophenyl, piperidine, and decanoate ester functional groups.*

FDA Label Image

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An illustration showing an injection vial with labeled features: a colored ring, a colored point, and the breaking level of the vial. The image likely indicates how to identify or open the vial for HALOPERIDOL DECANOATE injection.*

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An instructional line drawing showing two hands preparing an injection. One hand holds a syringe needle, with an arrow pointing to the needle tip, while the other hand holds the syringe barrel. The image likely illustrates the proper handling or preparation of the injection device for intramuscular use.*

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An instructional line drawing showing a person holding a small vial or ampule and snapping its neck to open it. The illustration focuses on the hands performing the action, likely related to preparation of an injection.*

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An instructional illustration showing a close-up of hands removing a cap or seal from the top of a vial or ampule, with an arrow indicating the direction to twist or pull. This likely depicts how to prepare HALOPERIDOL DECANOATE injection for use.*

FDA Label Image

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Label for Haloperidol Decanoate Injection 50 mg/mL in a 1 mL ampule, for intramuscular use only. Manufactured for Somerset Therapeutics, LLC in Hollywood, FL, made in India. Includes an NDC number and barcode, with space for expiration and lot number printing on a tear strip.*

FDA Label Image

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Packaging label for Haloperidol Decanoate Injection 50 mg/mL, 3 x 1 mL sterile ampules for intramuscular use. The label includes storage instructions, dosage form, strength, manufacturer Somerset Therapeutics LLC, and barcodes. The label is designed for a 3-ampule package and notes the product is Rx only.*

FDA Label Image

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Packaging label for Haloperidol Decanoate Injection 50 mg/mL, an intramuscular injection in 5 x 1 mL ampules. The label includes manufacturer information for Somerset Therapeutics, LLC. It states storage instructions, dosage form, strength, and usage directions, emphasizing protection from light and intramuscular use only.*

FDA Label Image

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Haloperidol Decanoate Injection 100 mg/mL label for intramuscular use, packaged as 1 mL ampules. Manufactured for Somerset Therapeutics, LLC, Hollywood, FL. The label includes the NDC number 70069-031-01 and indicates the product is made in India. A barcode and space for lot and expiration date overprinting are present.*

FDA Label Image

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Packaging label for Haloperidol Decanoate Injection 100 mg/mL, sterile solution in 1 mL ampules, for intramuscular use only. The label shows a package of 5 x 1-mL ampules, manufactured for Somerset Therapeutics LLC. It includes storage instructions, dosage form, and manufacturer information, along with barcodes and space for lot and expiration dates.*

FDA Label Image

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Label for Haloperidol Decanoate Injection 50 mg/mL, a 1 mL single-dose vial for intramuscular use only. Manufactured for Somerset Therapeutics, LLC, Hollywood, FL, and made in India. The label includes the NDC 70069-381-01 and a barcode, with instructions to keep an area blank for overprinting the lot number and expiration date.*

FDA Label Image

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Packaging label for Haloperidol Decanoate Injection 50 mg/mL, a single-dose vial for intramuscular use. The label includes the NDC 70069-381-01, manufacturer Somerset Therapeutics LLC, and storage instructions. It specifies the product is made in India and contains preservative information.*

FDA Label Image

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Packaging label for Haloperidol Decanoate Injection 50 mg/mL, an intramuscular injection supplied in 10 single-dose 1 mL vials. The label includes the manufacturer Somerset Therapeutics, LLC with contact information, storage instructions, and a note to retain vial in carton until use. Made in India, the product carries NDC 70069-381-10.*

FDA Label Image

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Label for Haloperidol Decanoate Injection 250 mg/5 mL (50 mg/mL) in a 5 mL multiple-dose vial for intramuscular use. Manufactured for Somerset Therapeutics, LLC, Hollywood, FL, and made in India. The label includes an NDC number and a barcode.*

FDA Label Image

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Haloperidol Decanoate Injection 250 mg/5 mL (50 mg/mL) in a carton label for 1 x 5 mL multiple-dose vial. The injection is for intramuscular use only and labeled with drug amount, NDC 70069-382-01, manufacturer Somerset Therapeutics, LLC, and storage instructions. The label also includes a barcode and preservative details.*

FDA Label Image

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Packaging label for Haloperidol Decanoate Injection 250 mg/5 mL (50 mg/mL) by Somerset Therapeutics LLC. The label indicates it is for intramuscular use only and comes in 5 x 5 mL multiple-dose vials. Storage instructions specify controlled room temperature and protection from light, with additional product composition and manufacturing details included.*

FDA Label Image

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Label for Haloperidol Decanoate Injection 100 mg/mL, 1 mL single-dose vial for intramuscular use. Manufactured for Somerset Therapeutics, LLC, Hollywood, FL. The label includes the NDC 70069-383-01 and a barcode, with instructions to keep the blue area blank for overprinting lot and expiration dates. Made in India.*

FDA Label Image

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Carton label for Haloperidol Decanoate Injection 100 mg/mL from Somerset Therapeutics LLC. The human prescription drug is presented in a 1 mL single-dose vial for intramuscular use. The label includes storage instructions, dosage form, and manufacturer details, with a prominent green box highlighting the 100 mg/mL strength.*

FDA Label Image

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Packaging label for Haloperidol Decanoate Injection 100 mg/mL, intramuscular use, manufactured by Somerset Therapeutics, LLC. The label indicates the product is supplied as 5 single-dose vials of 1 mL each, with storage instructions and ingredient details including haloperidol decanoate in sesame oil with benzyl alcohol as preservative. The label shows two barcodes and manufacturer contact information.*

FDA Label Image

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Haloperidol Decanoate Injection 100 mg/mL single-dose vial carton label showing product name, strength, and intramuscular use indication. Manufactured for Somerset Therapeutics, LLC with labeling including storage instructions, preservative information, and NDC 70069-383-10. Includes barcode and manufacturer details.*

FDA Label Image

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Label for Haloperidol Decanoate Injection 100 mg/mL (500 mg/5 mL) in a 5 mL multiple-dose vial. For intramuscular use only. Manufactured for Somerset Therapeutics, LLC, Hollywood, FL, and made in India. Includes barcode and lot/expiration date area instructions.*

FDA Label Image

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Packaging label for Haloperidol Decanoate Injection 500 mg/5 mL (100 mg/mL), an intramuscular injection by Somerset Therapeutics, LLC. The label indicates a 1 x 5 mL multiple-dose vial and includes storage, usage, and formulation information, highlighting that each mL contains 100 mg haloperidol decanoate in sesame oil with benzyl alcohol preservative.*

FDA Label Image

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Haloperidol Decanoate Injection 500 mg/5 mL (100 mg/mL) multidose vial label by Somerset Therapeutics LLC. The label indicates it is for intramuscular use only, with preservative benzyl alcohol in sesame oil vehicle, and storage instructions not to refrigerate or freeze. The package includes 5 x 5 mL multiple-dose vials.*

* 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.