Indium In 111 Chloride
Curium Us Llc
Human Prescription Drug
NDC 69945-132Indium In 111 Chloride is a human prescription drug labeled by 'Curium Us Llc'. National Drug Code (NDC) number for Indium In 111 Chloride is 69945-132. This drug is available in dosage form of Solution. The names of the active, medicinal ingredients in Indium In 111 Chloride drug includes Indium Chloride In-111 - 10 mCi/mL . The currest status of Indium In 111 Chloride drug is Active.
Drug Information:
| Drug NDC: | 69945-132 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Indium In 111 Chloride |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Prescription Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Indium In 111 Chloride |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Curium Us Llc |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Solution |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | INDIUM CHLORIDE IN-111 - 10 mCi/mL
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | INTRAVENOUS
|
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | NDA |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
| Marketing Start Date: | 07 Dec, 2007 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 18 Jan, 2026 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. |
| Application Number: | NDA019841 |
| This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null. |
| Listing Expiration Date: | 31 Dec, 2023 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | Curium US LLC
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UNII: | 58TD96H03I
|
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 69945-132-06 | 1 VIAL, GLASS in 1 CAN (69945-132-06) / .5 mL in 1 VIAL, GLASS | 07 Dec, 2007 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Product Elements:
Indium in 111 chloride indium in 111 chloride indium chloride in-111 indium cation in-111 hydrochloric acid
Indications and Usage:
Indications and usage indium in 111 chloride sterile solution is indicated for radiolabeling prostascint preparations used for in vivo diagnostic imaging procedures. it is also indicated for radiolabeling zevalin preparations used for radioimmunotherapy procedures. please refer to the package insert for prostascint or zevalin for information on the final drug product.
Warnings:
Warnings contents of the vial of indium in 111 chloride solution are intended only to be used as an ingredient for radiolabeling prostascint for use in in vivo diagnostic imaging procedures or to be used as an ingredient for radiolabeling zevalin⢠for use in radioimmunotherapy procedures, and are not to be administered directly to humans.
General Precautions:
General caution must be used to maintain proper aseptic technique while withdrawing and transferring contents of the indium chloride solution vial. do not use after expiration time and date indicated on vial label. contents of the vial are radioactive and adequate shielding and handling precautions must be maintained at all times.
Dosage and Administration:
Dosage and administration radiation dosimetry please refer to the package insert for prostascint or zevalin for this information on the final drug product.
Contraindications:
Contraindications please refer to the package insert for prostascint or zevalin for this information on the final drug product.
Adverse Reactions:
Adverse reactions please refer to the package insert for prostascint or zevalin for this information on the final drug product.
Use in Pregnancy:
Pregnancy category please refer to the package insert for prostascint or zevalin for this information on the final drug product.
Pediatric Use:
Pediatric use please refer to the package insert for prostascint or zevalin for this information on the final drug product.
Description:
Description indium in 111 chloride sterile solution is indicated for radiolabeling prostascint⢠preparations used for in vivo diagnostic imaging procedures. it is also indicated for radiolabeling zevalin⢠preparations used for radioimmunotherapy procedures. it is supplied as a sterile, non-pyrogenic solution of indium in 111 chloride in 0.05 molar hydrochloric acid. no carrier has been added to the solution. each 0.5 milliliter of the solution contains 185 megabequerels (5 millicuries) of indium in 111 chloride at time of calibration (specific activity of >1.85 gbq/μg indium; >50 mci/μg indium at this time of calibration). the solution ph is 1.1 to 1.4. radionuclidic purity indium in-111 is cyclotron produced by the proton irradiation ((p,2n) reaction) of cadmium cd-112 enriched target. at time of calibration, it contains not less than 99.925% indium in-111 and, not more than 0.075% indium in-114m and zinc zn-65 combined. at the time of expiration, it contains not less than 99.85% indium 111 and not more than 0.15% indium in-114m and zinc zn-65 combined. no carrier has been added. radiochemical purity at the time of calibration, the indium in 111 chloride sterile solution contains not less than 95% of the indium present as ionic in 3+ . chemical purity indium in 111 chloride sterile solution is tested for the following metallic impurities: copper, iron, cadmium, lead, zinc, nickel, and mercury, and contains extremely low levels of these metals. the sum of the individual impurity ratios for the metals listed is not more than 0.60 ppm. physical characteristics indium in-111 decays by electron capture to cadmium cd-111 (stable) with a physical half-life of 67.32 hours (2.81 days) ( see table 2 ) from radiopharmaceutical internal dosimetry information center, oak ridge associated universities, oak ridge, tn 37831-0117, february 1985. . photons useful for detection and imaging are listed in table 1 . table 1. principal radiation emission data * radiation mean percent per disintegration mean energy (kev) * kocher, david c., "radioactive decay data tables", doe/tic-11026, 115 (1981). gamma-2 90.2 171.3 gamma-3 94.0 245.4 external radiation the exposure rate constant for 37 mbq (1 mci) of indium in-111 is 8.3 x 10 -4 c/kg/hr (3.21 r/hr) at 1 cm. the specific gamma ray constant for indium in-111 is 3.21 r/hr-mci @ 1 cm . the first half-value thickness of lead (pb) is 0.023 cm. a range of values for the relative attenuation of the radiation emitted by this radionuclide that results from interposition of various thicknesses of pb is shown in table 2 . for example, the use of 0.834 cm of pb will decrease the external radiation exposure by a factor of about 1000. table 2. indium in-111 radiation attenuation by lead shielding shield thickness (pb) cm coefficient of attenuation 0.023 0.5 0.203 10 -1 0.513 10 -2 0.834 10 -3 1.12 10 -4 these estimates of attenuation do not take into consideration the presence of longer-lived contaminants with higher energy photons, namely indium in-114m. to correct for physical decay of indium in-111, the fractions that remain at selected intervals before and after calibration time are shown in table 3 . table 3. indium in-111 physical decay chart; half-life 67.32 hours (2.81 days) * calibration time hours fraction remaining hours fraction remaining -72 2.10 0* 1.00 -60 1.85 6 0.94 -48 1.64 12 0.88 -36 1.45 24 0.78 -24 1.28 36 0.69 -12 1.13 48 0.61 -6 1.06 72 0.48
Clinical Pharmacology:
Clinical pharmacology please refer to the package insert for prostascint or zevalin for this information on the final drug product.
Carcinogenesis and Mutagenesis and Impairment of Fertility:
Carcinogenesis, mutagenesis, impairment of fertility please refer to the package insert for prostascint or zevalin for this information on the final drug product.
How Supplied:
How supplied indium in 111 chloride sterile solution is supplied in 10 ml vials containing 0.5 ml of solution. it is a sterile non-pyrogenic solution in 0.05 molar hydrochloric acid. no carrier is added to the solution. each 0.5 ml contains 185 megabequerels (5 millicuries) of indium in 111 chloride at time of calibration. the ph of the solution is 1.1 to 1.4. special storage and handling the contents of the vial are radioactive and adequate shielding and handling precautions must be maintained. store at controlled room temperature 20° to 25°c (68° to 77°f) [see usp]. storage and disposal of indium in 111 chloride sterile solution should be controlled in a manner that is in compliance with the appropriate regulations of the government agency authorized to license the use of the radionuclide. the vial should be kept inside its transportation shield whenever possible and should be handled with forceps when contents are being removed. pharmacovigilance:1-866-789-2211 prostasci
Read more...nt is a trademark of eusa pharma (usa), inc. zevalin is a trademark of rit oncology, llc. curium and the curium logo are trademarks of a curium company. ©2018 curium us llc. all rights reserved. manufactured by: curium us llc maryland heights, mo 63043 made in usa a132i0 r12/2018 curium tm
Package Label Principal Display Panel:
Principal display panel indium in 111 chloride sterile solution sterile, non-pyrogenic solution contains no bacteriostatic preservative store at controlled room temperature 20° to 25°c (68° to 77°f) single dose - not for direct administration no carrier added for use only in radiolabeling prostascint⢠(capromab pendetide), and zevalin⢠(ibritumomab tiuxetan) see package insert for information rx only warning: radioactive drugs must be handled only by qualified personnel in conformity with regulations of the u.s. nuclear regulatory commission or state regulatory agencies where applicable. bottle containing drug should be kept in this container or within heavier shield. manufactured by: curium us llc maryland heights, mo 63043 made in usa curium tm caution radioactive material a132c0 r12/2018 a132c0-cn0000-us122018 spl a132c0-cn0000-us122018