Bupivacaine Hydrochloride Injection, Solution
Product Images NDC 70069-752

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Bupivacaine Hydrochloride (NDC 70069-752). 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 Bupivacaine hydrochloride depicting its molecular composition including the hydrochloride and water components.*

FDA Label Image

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Label for Bupivacaine Hydrochloride Injection, USP 0.25% (2.5 mg/mL), 125 mg/50 mL multiple-dose vial. The label states it is for infiltration and nerve block, but not for caudal, epidural, or intrathecal anesthesia. Manufactured for Somerset Therapeutics, LLC, Hollywood, FL. The vial is made in India.*

FDA Label Image

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Packaging label for Bupivacaine Hydrochloride Injection, USP 0.25% (2.5 mg/mL) by Somerset Therapeutics, LLC. The label is for 125 mg/50 mL (2.5 mg/mL) solution in multiple-dose vials, 25 vials of 50 mL each. It specifies use for infiltration and nerve block, excluding caudal, epidural, or intrathecal anesthesia. Manufactured in India, the product is clear and colorless and includes storage instructions.*

FDA Label Image

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Label for Bupivacaine Hydrochloride Injection, USP 0.5% (5 mg/mL) with a total content of 250 mg per 50 mL multiple-dose vial. Intended for nerve block use, specifically stating it is not for caudal, epidural, or intrathecal anesthesia. Manufactured for Somerset Therapeutics, LLC in Hollywood, FL, with the product made in India. Includes storage and preservative information along with a barcode and lot/expiration placeholders.*

FDA Label Image

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Label for Bupivacaine Hydrochloride Injection USP 0.5% (5 mg/mL) in a multiple-dose vial package of 25 x 50 mL. The label indicates the total quantity as 250 mg per 50 mL, for nerve block use, not for caudal, epidural, or intrathecal anesthesia. Manufactured for Somerset Therapeutics, LLC with detailed storage instructions and a customer care contact.*

FDA Label Image

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Label for Bupivacaine Hydrochloride Injection USP 0.25%, 125 mg/50 mL (2.5 mg/mL) multiple-dose vials. Injection solution for infiltration and nerve block, not for caudal, epidural, or intrathecal anesthesia. Manufactured for Somerset Therapeutics, LLC, Hollywood, FL. Includes storage instructions and product clarity note.*

FDA Label Image

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Packaging label for Bupivacaine Hydrochloride Injection USP 0.25% (2.5 mg/mL) in a 50 mL multiple-dose vial. The label, manufactured for Somerset Therapeutics, LLC, indicates the product is for infiltration and nerve block, not for caudal, epidural, or intrathecal anesthesia. Additional storage and composition details are included on the label along with a barcode and contact information.*

FDA Label Image

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Packaging label for Bupivacaine Hydrochloride Injection, USP 0.5%, containing 250 mg per 50 mL (5 mg/mL) in a multiple-dose vial. The label indicates use for nerve block and states it is not for caudal, epidural, or intrathecal anesthesia. Manufactured for Somerset Therapeutics, LLC, Hollywood, FL, with storage instructions and preservative information included.*

FDA Label Image

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Label for Bupivacaine Hydrochloride Injection, USP 0.5% (5 mg/mL) multiple-dose vial, 50 mL, containing 250 mg per vial. The label specifies use for nerve block and states it is not for caudal, epidural, or intrathecal anesthesia. Manufactured for Somerset Therapeutics, LLC, Hollywood, FL. Includes storage instructions and ingredient information. Contains antiseptic preservative methylparaben and is made in India.*

* 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.