Ropivacaine Hydrochloride Injection
Product Images NDC 70069-063

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 21 technical images submitted to the FDA as part of the official labeling for Ropivacaine Hydrochloride (NDC 70069-063). 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 diagram of Ropivacaine Hydrochloride monohydrate with molecular formula C17H26N2O·HCl·H2O and molecular weight 328.89.*
FDA Label Image

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Ropivacaine HCl Injection, USP 0.2% (2 mg/mL) in a 10 mL single-dose vial. The label states the product is for infiltration, nerve block, and epidural administration only, not for intravenous use. Manufactured for Somerset Therapeutics, LLC, Hollywood, FL, and made in India. The label includes storage instructions and ingredients per mL.*
FDA Label Image

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Label for Ropivacaine HCl Injection, USP 0.2% (2 mg/mL) by Somerset Therapeutics, LLC. The label identifies the product as a 25 x 10 mL single-dose vial pack made in India. It specifies administration routes: infiltration, nerve block, and epidural only, not for intravenous use. Storage instructions and manufacturing information are also included.*
FDA Label Image

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Label for Ropivacaine HCl Injection USP 0.2% (40 mg/20 mL, 2 mg/mL) single-dose vial. Indicated for infiltration, nerve block, and epidural administration only. Manufactured for Somerset Therapeutics, LLC, Hollywood, FL. Contains Ropivacaine HCl 2 mg per mL with sodium chloride and pH adjusters. Storage recommended at 20° to 25°C.*
FDA Label Image

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Label for Ropivacaine HCl Injection, USP 0.2% (40 mg/20 mL, 2 mg/mL) by Somerset Therapeutics, LLC. The label indicates the product is a single-dose vial (25 x 20 mL) intended for infiltration, nerve block, and epidural administration only. It includes storage instructions, manufacturer information, and warnings that the container is single-dose and preservative-free.*
FDA Label Image

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Label for Ropivacaine HCl Injection, USP 0.5% (5 mg/mL) in a 20 mL single-dose vial supplied by Somerset Therapeutics, LLC. It contains 100 mg of ropivacaine hydrochloride per 20 mL vial and is indicated for infiltration, nerve block, and epidural administration, not for intravenous use. Storage instructions and manufacturing details including origin in India are also shown.*
FDA Label Image

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Carton label for Ropivacaine HCl Injection, USP 0.5% strength (5 mg/mL) by Somerset Therapeutics, LLC. The label indicates a 100 mg/20 mL (5 mg/mL) single-dose vial format. It specifies usage for infiltration, nerve block, and epidural administration only, with no intravenous administration. The label includes manufacturer information, storage instructions, and a barcode.*
FDA Label Image

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Label for Ropivacaine HCl Injection, USP 0.5% (5 mg/mL) in a 30 mL single-dose vial. The label states a total of 150 mg per 30 mL and indicates the drug is for infiltration, nerve block, and epidural administration only, not for intravenous use. It is manufactured for Somerset Therapeutics, LLC, Hollywood, FL.*
FDA Label Image

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Label for Ropivacaine HCl Injection, USP 0.5% (5 mg/mL) in a 30 mL single-dose vial, providing 150 mg per vial. The label states the drug is for infiltration, nerve block, and epidural administration only, not for intravenous use. Manufactured by Somerset Therapeutics, LLC, with storage instructions and formulation details including the absence of preservatives and a pH range of 4.0 to 6.0.*
FDA Label Image

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Label for Ropivacaine HCl Injection, USP 0.75% (7.5 mg/mL) in a 20 mL single dose vial. The label states use for infiltration, nerve block, and epidural administration only, not for intravenous use. Manufactured for Somerset Therapeutics, LLC. Includes storage instructions, ingredients, and a barcode.*
FDA Label Image

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Ropivacaine HCl Injection, USP 0.75% (7.5 mg/mL) solution in 20 mL single-dose vials, with a total of 150 mg per vial. Label includes dosing and storage instructions, ingredient details, and indicates it is manufactured by Somerset Therapeutics LLC, Hollywood, FL. The product is for infiltration, nerve block, and epidural administration only.*
FDA Label Image

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Label for Ropivacaine HCl Injection, USP 1% (10 mg/mL), 100 mg/10 mL single-dose vial for epidural administration only. Each mL contains 10 mg Ropivacaine HCl with sodium chloride and pH adjusters. Manufactured by Somerset Therapeutics, LLC in Hollywood, FL. Storage recommended at 20° to 25°C (68° to 77°F).*
FDA Label Image

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Ropivacaine HCl Injection, USP 1% (10 mg/mL) vial label for 25 x 10 mL single-dose vials by Somerset Therapeutics, LLC. The label states the drug is for epidural administration only and not for intravenous use. It contains ingredient and storage information, manufacturer details including Made in India, and barcodes on the label.*
FDA Label Image

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Label for Ropivacaine HCl Injection, USP 1% (10 mg/mL) in a 20 mL single-dose vial. The label states 200 mg per 20 mL and specifies use for epidural administration only, not intravenous. Manufactured for Somerset Therapeutics, LLC, Hollywood, FL, and made in India. Includes storage instructions and ingredients per mL.*
FDA Label Image

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Packaging label for Ropivacaine HCl Injection, USP 1% strength, 200 mg/20 mL (10 mg/mL) in single-dose vials. The label indicates administration by epidural only and warns against intravenous use. Manufactured by Somerset Therapeutics, LLC, with storage instructions and ingredient details included. The label features a barcode and space for lot and expiration date printing.*
FDA Label Image

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Ropivacaine HCl Injection, USP 0.5% (5 mg/mL) in a 150 mg/30 mL vial. The label indicates it is for infiltration, nerve block, and epidural administration only, not for intravenous use. Manufactured for Somerset Therapeutics, LLC. The package contains 10 single-dose vials of 30 mL each.*
FDA Label Image

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Carton label for Ropivacaine HCl Injection, USP 0.5% (5 mg/mL), with a total of 150 mg/30 mL. The label indicates it is for infiltration, nerve block, and epidural administration only, not for intravenous use. Manufactured for Somerset Therapeutics, LLC, Hollywood, FL, with a barcode and storage instructions included. The label also notes no preservatives and single dose container.*
FDA Label Image

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Label for Ropivacaine HCl Injection, USP 0.2% (2 mg/mL), 20 mg/10 mL single-dose vials. The label states it is for infiltration, nerve block, and epidural administration only, not for intravenous use. Manufactured by Somerset Therapeutics, LLC, the label includes barcodes, storage instructions, and product composition details.*
FDA Label Image

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The label for Ropivacaine HCl Injection, USP 0.2% (2 mg/mL), presenting a 40 mg/20 mL single-dose vial packaging. It includes formulation details, manufacturer Somerset Therapeutics LLC, storage instructions, and usage restrictions for epidural, infiltration, and nerve block administration. The label features barcodes and lot/expiration placeholders.*
FDA Label Image

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Label for Ropivacaine HCl Injection, USP 1% (10 mg/mL) in a 10 mL single-dose vial, manufactured by Somerset Therapeutics, LLC. The label includes active ingredient details, storage instructions, and specifies use for epidural administration only, not intravenous. It also states the product is made in India and is prescription only.*
FDA Label Image

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Ropivacaine HCl Injection, USP 1% (10 mg/mL) 200 mg/20 mL vial, single-dose, in a package of 10 vials. Label indicates use for epidural administration only and not for intravenous use. Manufactured for Somerset Therapeutics, LLC. Storage instructions and formulation details are included on the label along with the NDC 70069-067-10 barcode.*

* 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.