Tissueblue

Brilliant Blue G


D.o.r.c. Dutch Ophthalmic Research Center (international) B.v.
Human Prescription Drug
NDC 68803-722
Tissueblue also known as Brilliant Blue G is a human prescription drug labeled by 'D.o.r.c. Dutch Ophthalmic Research Center (international) B.v.'. National Drug Code (NDC) number for Tissueblue is 68803-722. This drug is available in dosage form of Injection, Solution. The names of the active, medicinal ingredients in Tissueblue drug includes Brilliant Blue G - .0125 mg/.5mL . The currest status of Tissueblue drug is Active.

Drug Information:

Drug NDC: 68803-722
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: Tissueblue
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: Brilliant Blue G
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: D.o.r.c. Dutch Ophthalmic Research Center (international) B.v.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Injection, 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:BRILLIANT BLUE G - .0125 mg/.5mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:INTRAOCULAR
OPHTHALMIC
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: 31 Dec, 2019
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: NDA209569
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:D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
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:M1ZRX790SI
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 NDCDescriptionMarketing Start DateMarketing End DateSample Available
68803-722-0510 POUCH in 1 CARTON (68803-722-05) / 1 SYRINGE, GLASS in 1 POUCH / .5 mL in 1 SYRINGE, GLASS31 Dec, 2019N/ANo
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:

Tissueblue brilliant blue g polyethylene glycol 3350 sodium chloride sodium phosphate, dibasic, dodecahydrate sodium phosphate, monobasic, dihydrate water brilliant blue g brilliant blue g

Indications and Usage:

Tissueblue 0.025% - indications & usage section tissueblue (brilliant blue g ophthalmic solution) 0.025% is is a disclosing agent indicated to selectively stain the internal limiting membrane (ilm). tissueblue (brilliant blue g ophthalmic solution) 0.025% is is a disclosing agent indicated to selectively stain the internal limiting membrane (ilm).

Warnings and Cautions:

Tissueblue 0.025% - warnings and precautions section excessive staining excess tissueblue 0.025% should be removed from the eye immediately after staining. use of the syringe make sure the plunger moves smoothly before injecting the solution. do not use the product if the plunger does not move smoothly to prime the cannula. excessive staining: excess tissueblue 0.025% should be removed from the eye immediately after staining. use of the syringe: make sure the plunger moves smoothly before injecting the solution.

Dosage and Administration:

Tissueblue 0.025% - dosage & administration section tissueblue 0.025% is carefully injected into the balanced salt solution (bss)-filled vitreous cavity using a blunt cannula attached to the pre-filled syringe, without allowing the cannula to contact the retina or allowing tissueblue to get under the retina. sufficient staining is expected within a few seconds. following staining, all excess dye should be removed from the vitreous cavity. inject tissueblue 0.025% directly in a balanced salt solution (bss)-filled vitreous cavity. excess tissueblue should be removed from the vitreous cavity.

Dosage Forms and Strength:

Tissueblue 0.025% - dosage forms & strengths section tissueblue (brilliant blue g ophthalmic solution) 0.025% is a clear, bright blue, single-dose ophthalmic solution supplied in 2.25 ml syringes pre-filled to a volume of 0.5 ml. tissueblue (brilliant blue g ophthalmic solution) 0.025% is supplied in 2.25 ml syringes filled to a volume of 0.5 ml.

Contraindications:

Tissueblue 0.025% - contraindications section none none

Adverse Reactions:

Tissueblue 0.025% - adverse reactions section adverse reactions that have been reported in procedures that included the use of brilliant blue g ophthalmic solution have often been associated with the surgical procedure. these complications include retinal (retinal break, tear, hemorrhage, and detachment) and cataracts. adverse reactions that have been reported in procedures that included the use of tissueblue 0.025% have often been associated with the surgical procedure. the complications include retinal (retinal break, tear, hemorrhage, and detachment and cataracts. to report suspected adverse reactions, contact dutch ophthalnic, usa at 1-800-75-dutch or fda at 1-800-fda-1088 or www.fda.gov/medwatch

Use in Specific Population:

Tissueblue 0.025% - use in specific populations section tissueblue 0.025% - pregnancy section risk summary there are no available data on the use of tissueblue 0.025% in pregnant women to inform a drug associated risk. systemic absorption of tissueblue 0.025% in humans is expected to be negligible following intravitreal injection and subsequent removal of the drug at the completion of surgical procedures. due to the negligible systemic exposure, it is not expected that maternal use of tissueblue 0.025% will result in fetal exposure to the drug. adequate animal reproduction studies were not conducted with tissueblue 0.025%. tissueblue 0.025% - lactation section risk summary no data are available regarding the presence of brilliant blue g in human milk after intraocular administration of tissueblue 0.025%, or the effects on the breastfed infant or the effects on milk production. however, breastfeeding is not expected to result in exposure of the child to brilliant blue g due to the expec
ted negligible systemic exposure of bbg in humans following intravitreal injection and subsequent removal of the drug at the completion of surgical procedures. tissueblue 0.025% - pediatric use section the safety and effectiveness of tissueblue 0.025% in pediatric patients has not been established. tissueblue 0.025% - geriatric use section no overall differences in safety or effectiveness were observed between elderly and younger adult patients.

Use in Pregnancy:

Tissueblue 0.025% - pregnancy section risk summary there are no available data on the use of tissueblue 0.025% in pregnant women to inform a drug associated risk. systemic absorption of tissueblue 0.025% in humans is expected to be negligible following intravitreal injection and subsequent removal of the drug at the completion of surgical procedures. due to the negligible systemic exposure, it is not expected that maternal use of tissueblue 0.025% will result in fetal exposure to the drug. adequate animal reproduction studies were not conducted with tissueblue 0.025%.

Pediatric Use:

Tissueblue 0.025% - pediatric use section the safety and effectiveness of tissueblue 0.025% in pediatric patients has not been established.

Geriatric Use:

Tissueblue 0.025% - geriatric use section no overall differences in safety or effectiveness were observed between elderly and younger adult patients.

Description:

Tissueblue 0.025% - description section tissueblue (brilliant blue g ophthalmic solution) 0.025% is a sterile solution of bbg (a dye). each ml of tissueblue 0.025% contains bbg 0.25 mg, polyethylene glycol 40mg and buffered sodium chloride solution (8.20 mg of sodium chloride, 3.10 mg sodium phosphate dibasic dodecahydrate, 0.30 mg sodium phosphate monobasic dihydrate, water for injection). the ph range of tissueblue 0.025% solution is between 7.3 and 7.6. the drug substance bbg has the chemical name brilliant blue g, a molecular weight of 854.02 and has the following chemical structure: molecular formula: c 47 h 48 n 3 nao 7 s 2 chemical structure tissueblue

Clinical Pharmacology:

Tissueblue 0.025% - clinical pharmacology section tissueblue 0.025% - mechanism of action section brilliant blue g has been shown to selectively stain the ilm, but not the epiretinal membrane nor the retina, making it easier to visualize the membrane for removal, although the exact mechanism of this selectivity has not been elucidated.

Mechanism of Action:

Tissueblue 0.025% - mechanism of action section brilliant blue g has been shown to selectively stain the ilm, but not the epiretinal membrane nor the retina, making it easier to visualize the membrane for removal, although the exact mechanism of this selectivity has not been elucidated.

Nonclinical Toxicology:

Tissueblue 0.025% - nonclinical toxicology section tissueblue 0.025% - nonclinical toxicology section studies to evaluate the potential for carcinogenicity or impairment of fertility of tissueblue 0.025% have not been conducted. brilliant blue g was not mutagenic in the ames assay, the in vitro mouse lymphoma assay, or the in vivo rat micronucleus assay.

Tissueblue 0.025% - nonclinical toxicology section studies to evaluate the potential for carcinogenicity or impairment of fertility of tissueblue 0.025% have not been conducted. brilliant blue g was not mutagenic in the ames assay, the in vitro mouse lymphoma assay, or the in vivo rat micronucleus assay.

How Supplied:

Tissueblue 0.025% - how supplied section tissueblue (brilliant blue g ophthalmic solution), 0.025% is supplied as 0.5 ml of brilliant blue g ophthalmic solution, 0.025% in a sterile, single-dose luer lok, 2.25 ml glass syringe, with a grey rubber plunger stopper and tip cap with polypropylene plunger rod in a pre-formed polypropylene blister pouch sealed with a tyvek® lid. ndc 68803-722-05 (one 0.5 ml syringe) ndc 68803-722-25 (carton of five 0.5 ml syringes)

Package Label Principal Display Panel:

Package label - 0.5 ml tissueblue (brilliant blue g ophthalmic solution) 0.025% staining solution for ophthalmic surgery protect from light, frost and moisture. store at 15°c to 25°c (59°f to 77°f). sterile. active ingredients/ingrédient actif: brilliant blue g 0.025% inactive ingredients/ingrédients inactifs: water for injection, sodium chloride, sodium phosphate dibasic dihydrate, sodium phosphate monobasic dihydrate, polyethylene glycol. ndc 68803-722-05 (one 0.5 ml syringe) ndc 68803-722-25 (carton of five 0.5 ml syringes) tissuebluebox.jpg


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