Product Images Ropivacaine Hydrochloride

This appears to be a chemical formula and molecular weight information, but it is not clear what molecule is being referred to. Without further context, it is difficult to provide a more specific description.*

This is a description of a medication called Ropivacaine HCI. It is an injection used for infiltration, nerve block, and epidural administration. It should not be used for intravenous administration. The medication is contained in a single-dose vial of 10 mL and each mL contains 2 mg of Ropivacaine HCI, 8.6 mg of sodium chloride, and sodium hydroxide and/or hydrochloric acid to adjust the pH to 4.0 to 6.0. The medication should be stored at 20° to 25°C (68° to 77°F). It was manufactured in India and is distributed by Somerset Therapeutics, LLC in Hollywood, FL. The code number is KR/DRUGS/KTK/28/289/97 and the lot and expiration information can be overprinted onto the area provided.*

This is a prescription drug with the National Drug Code (NDC) of 70069-062-01. It is an injection of 40 mg/20 mL (2 mg/mL) of Ropivacaine HCI, USP, to be used for infiltration, nerve block, and epidural administration only. It is not for intravenous administration. Each mL of the injection contains Ropivacaine HCI 2 mg, Sodium Chloride 8.6 mg, Sodium hydroxide, and/or hydrochloric acid to adjust pH to 4.0 to 6.0. It is stored at a temperature range of 20°C to 25°C (68°F to 77°F). The injection is manufactured for Somerset Therapeutics, LLC and is made in India. The code number is KR/DRUGS/KTK/28/289/97, and the LOT number is to be overprinted in the blank and varnish-free area.*

This is a description of a medication called Ropivacaine HCI injection USP. It comes in a 20 mL single-dose vial containing 100 mg of the medication per 20 mL, with each mL containing 5 mg of Ropivacaine HCI, 8 mg of Sodium chloride, and Sodium hydroxide and/or hydrochloric acid for pH adjustment. This injection is meant for Infiltration, Nerve Block, and Epidural Administration, and should not be used for Intravenous Administration. The medication should be stored at 20° to 25°C (68° to 77°F). The medication is produced by Somerset Therapeutics, LLC, in Hollywood, FL 33024, and is marked with the code ST-ROP21/L/01. The medication is made in India with the code No.:KR/DRUGS/KTK/28/289/97.*

This is a description of a single-dose vial of Ropivacaine HCI injection, USP containing 150 mg in 30 mL with a concentration of 5 mg/mL. The vial is intended for infiltration, nerve block, and epidural administration only and should not be used for intravenous administration. Each milliliter of the solution contains 5mg of Ropivacaine HCI, 8mg of Sodium chloride, and Sodium hydroxide and/or hydrochloric acid to adjust pHto 4.0t0 6.0. The vial does not contain any preservatives and the unused portion should be discarded. Storage should be done at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. It is manufactured for Somerset Therapeutics, LLC and made in India.*

This is a description of a medication with the NDC code 70069-065.01. It is a prescription medicine called Ropivacaine HCI and is available in a 150 mg/20 mL (7.5 mg/ml) single-dose vial for administration through infusion, nerve block, or epidural routes only. It is not meant for intravenous administration. Each mL of the medicine contains Ropivacaine HCI 7.5 mg, Sodium chloride 7.5 mg, and Sodium hydroxide and/or hydrochloric acid to adjust the pH. The medicine must be stored at 20° to 25°C (68° to 77°F) in a controlled room temperature according to USP standards. It is manufactured for Somerset Therapeutics, LLC, located in Hollywood, FL 33024, and made in India. No further information is provided about the medicine.*

This is a description of a medication package containing 25 single dose vials of Ropivacaine HCI injection. The medication is intended for use as nerve block or epidural administration only, not for intravenous administration. The solution contains Ropivacaine HCI 7.5gm, Sodium chloride 7.5mg, and Sodium hytrosde andlor hythochoro acid. The container closure is not made with natural rubber latex. The package includes storage instructions and information on how to use the medication safely. Made in India by Somerset Therapeutics. The code number is KRDRUGSKTK28289/97.*

NDC 70069-066-01 is an Rxonly injection containing Ropivacaine HCI and Sodium chloride for Epidural administration only. It is not for Intravenous administration. Each mL contains Ropivacaine HCI 10 mg, Sodium chloride and Ropivacaine HCI 7.1 mg, Sodium hydroxide and/or hydrochloric acid to adjust pH to 4.0 to 6.0. It is stored at 20° to 25°C (68° to 77°F) and manufactured in India by Somerset Therapeutics, LLC. The 10 mL Single-Dose Vial Code No. is KR/DRUGS/KTK/28/289/97.*

This appears to be a label of a drug named Ropivacaine HCI Injection, USP. It contains specific information such as the quantity, concentration, and usage of the drug. It also mentions the manufacturer and instruction for storage. The label instructs to discard unused portions and warns that the container is made with natural rubber. However, it is not clear why the text contains the name "dan" and "At xmm."*

This is a description of a medication with the National Drug Code (NDC) 70069-067-01, intended for epidural administration only, with a concentration of 10mg/mL of Ropivacaine HCI in a 20mL single-dose vial. The solution contains 10mg of Ropivacaine HCI, 7.1mg of sodium chloride, and hydrochloric acid to adjust the pH to 4.0-6.0. It is manufactured for Somerset Therapeutics and not intended for intravenous administration. The medication is stored at temperatures between 68-77°F. Made in India.*

Ropivacaine HCI injection is a solution indicated for Infiltration, Nerve Block, and Epidural Administration. Each mL contains Ropivacaine HCI 5 mg, Sodium chloride 8 mg, Sodium hydroxide, and hydrochloric acid to adjust pH 10 4.0 106.0. The solution is contained in a single-dose container and has no preservatives. The prescribed dosage should be consulted for proper use. The solution can be autoclaved, and it should not be used if it is discolored or contains a precipitate. The container closure does not contain natural rubber latex. It is manufactured in India for Somerset Therapeutics, LLG, based in Hollywood, FL 33024.*

This is a description of a drug solution container manufactured by Somerset Therapeutics LLC. The solution contains Ropivacaine HCI, Sodium chloride, and Sodium hydroxide/hydrochloric acid to adjust the pH. It is a single-dose container and is not for intravenous administration. The storage requirements for the solution are at a controlled room temperature between 20 to 25°C. The package insert should be consulted for dosage and other prescribing information.*

This is a description of a medical product called Ropivacaine HCI Injection, USP. It is a solution that can be administered through intravenous, nerve block, or epidural routes. The solution comes in packages of 598 with instructions. It is recommended to be stored between 20 and 25 degrees Celsius. It is advised not to use the solution if it is discolored or contains precipitates. The package contains 2 mg/ml of the solution.*

This is a description of a medication called "Ropivacaine HCI Injection, USP" manufactured by Somerset Therapeutics LLC. It is a single-dose container and contains 2g of Ropiacaine HCI, 0.6mg of Sodum choide, Sodium hydaide, and lorydrooloro acid o acst. The package contains 10x20mL Single-Dose Vials, and it is intended for nerve block, epidural administration, and infiltration only. The solution can be autoclaved but should not be used if the solution is discolored or containing precipitate. Prescription use only and not for intravenous administration. The storage temperature range is 20°to 25°C (68t 77°F).*

This is a description of a medication called Ropivacaine HCI Injection, USP. It comes in 10 mL single-dose vials and is used for epidural administration only, not intravenous administration. It contains 10 mg of Ropivacaine HCI, 7.1 mg of sodium chloride, and other chemicals to adjust the pH of the solution. It does not contain any preservatives and should be discarded if unused. It is manufactured by Somerset Therapeutics in India and is only available with a prescription. The container closure does not contain natural rubber latex. Storage should be at 20-25°C.*