Bupivacaine Hydrochloride Injection, Solution
Product Images NDC 70069-753

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Bupivacaine Hydrochloride (NDC 70069-753). 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 monohydrate, depicted with atomic connectivity including a piperidine ring, aromatic ring with methyl substituents, and associated hydrochloride and water molecules.*

FDA Label Image

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Label for Bupivacaine Hydrochloride Injection, USP 0.25% (2.5 mg/mL), 125 mg/50 mL in a 50 mL multiple-dose vial. Indicated for infiltration and nerve block, but not for caudal, epidural, or intrathecal anesthesia. Manufactured for Somerset Therapeutics, LLC, Hollywood, FL. Contains additional formulation and storage information, with barcodes and lot/expiration fields.*

FDA Label Image

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Packaging label for Bupivacaine Hydrochloride Injection, USP 0.25%, 125 mg/50 mL (2.5 mg/mL) multiple-dose vials by Somerset Therapeutics, LLC. The label states the product is for infiltration and nerve block, with instructions to avoid caudal, epidural, or intrathecal anesthesia. It includes storage instructions and manufacturing details.*

FDA Label Image

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

FDA Label Image

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The label for Bupivacaine Hydrochloride Injection, USP 0.5% (5 mg/mL), in a 25 x 50 mL multiple-dose vial package. The label states the drug is for nerve block and not for caudal, epidural, or intrathecal anesthesia. Manufactured for Somerset Therapeutics, LLC, the label includes dosage and storage instructions and shows the NDC 70069-753-25.*

* 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.