Dehydrated Alcohol

Alcohol


Bpi Labs, Llc
Human Prescription Drug
NDC 54288-105
Dehydrated Alcohol also known as Alcohol is a human prescription drug labeled by 'Bpi Labs, Llc'. National Drug Code (NDC) number for Dehydrated Alcohol is 54288-105. This drug is available in dosage form of Injection, Solution. The names of the active, medicinal ingredients in Dehydrated Alcohol drug includes Alcohol - 1 mL/mL . The currest status of Dehydrated Alcohol drug is Active.

Drug Information:

Drug NDC: 54288-105
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: Dehydrated Alcohol
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: Alcohol
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Bpi Labs, Llc
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:ALCOHOL - 1 mL/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:PERCUTANEOUS
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: 24 Oct, 2018
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 25 Dec, 2025
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: NDA207987
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:BPI Labs, LLC
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:2048979
2048982
The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
UPC:0354288105019
0354288105026
UPC stands for Universal Product Code.
UNII:3K9958V90M
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
54288-105-1010 AMPULE in 1 CARTON (54288-105-10) / 1 mL in 1 AMPULE (54288-105-01)24 Oct, 2018N/ANo
54288-105-1510 AMPULE in 1 CARTON (54288-105-15) / 5 mL in 1 AMPULE (54288-105-02)24 Oct, 2018N/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:

Dehydrated alcohol alcohol alcohol alcohol

Indications and Usage:

1 indications and usage ablysinol ® is indicated to induce controlled cardiac septal infarction to improve exercise capacity in adults with symptomatic hypertrophic obstructive cardiomyopathy who are not candidates for surgical myectomy. ablysinol is an ablative agent indicated to induce controlled cardiac septal infarction to improve exercise capacity in adults with symptomatic hypertrophic obstructive cardiomyopathy who are not candidates for surgical myectomy. ( 1 )

Warnings and Cautions:

5 warnings and precautions transient heart block: transient heart block is common at the time of injection. a temporary pacing wire is routinely inserted to mitigate transient heart block. (5.1) persistent heart block: approximately 10% of complete heart block events become permanent and require placement of a permanent pacemaker. (5.1) remove the temporary pacemaker lead if no episode of high-degree atrioventricular block occurs. (5.1) monitor the patient for heart failure, chest pain, and arrhythmias several days after the procedure. (5.1, 5.2 , 5.3 ) 5.1 heart block transient heart block transient heart block is common at the time of dehydrated alcohol, such as ablysinol, injection into a septal artery. prior to the injection, a temporary pacing wire is routinely inserted into the apex of the right ventricle, usually via the femoral vein, to treat transient heart block. the pacing lead can be removed if no episode of high-degree atrioventricular block occurs, usually after several h
ours of observation following percutaneous transluminal septal myocardial ablation. persistent heart block approximately 10% of complete heart block events become permanent and require placement of a permanent pacemaker following percutaneous transluminal septal myocardial ablation. risk factors for permanent pacemaker dependency after septal ablation include a baseline pq interval > 160 ms, baseline minimum heart rate < 50 bpm, baseline left ventricular outflow gradient > 70 mmhg, maximum qrs during the first 48 hours > 155 ms, 3rd degree atrio-ventricular block occurring during the procedure, and no clinical recovery between 12-48 hours after the procedure. 5.2 myocardial infarction injection of dehydrated alcohol is intended to create a controlled myocardial infarction for therapeutic purposes. however, excessive myocardial necrosis and subsequent heart failure have been reported. factors increasing the risk of excessive tissue necrosis include higher volume of alcohol used and a higher number of septal branches injected to reduce the left ventricular outflow tract gradient. 5.3 ventricular arrhythmia ventricular tachycardia and ventricular fibrillation requiring electrocardioversion occurred at a frequency of approximately 1%. perform continuous electrocardiographic monitoring for 48 hours after the procedure.

Dosage and Administration:

2 dosage and administration inject small volumes over 1 to 2 minutes percutaneously into septal arterial branches, using the minimal dose necessary to achieve the desired reduction in peak left ventricular outflow tract pressure gradient. ( 2.1 ) in most situations, a dose of 1 ml to 2 ml is sufficient. the maximum dose that should be used in a single procedure is 5 ml. ( 2.1 ) 2.1 recommended dosing use the minimum dose necessary to achieve the desired reduction in peak left ventricular outflow tract pressure gradient. inject small volumes over 1 to 2 minutes percutaneously into septal arterial branches, guided by assessment of the gradient. in most situations, a dose of 1 ml to 2 ml is sufficient. the maximum dose of ablysinol that should be used in a single procedure is 5 ml. 2.2 administration ablysinol should only be administered under the supervision of a qualified interventional cardiologist experienced in the percutaneous transluminal septal myocardial ablation procedure. inspe
ct visually for particulate matter and discoloration prior to administration. ablysinol should appear as a clear, colorless solution.

Dosage Forms and Strength:

3 dosage forms and strengths injection: 1 ml or 5 ml of ethyl alcohol ≥ 99% by volume as a clear, colorless liquid in a single-dose glass ampule. injection: 1 ml or 5 ml of ethyl alcohol ≥ 99% by volume as a clear, colorless liquid in a single-dose glass ampule. ( 3 )

Contraindications:

4 contraindications none. none ( 4 )

Adverse Reactions:

6 adverse reactions heart block [ see warnings and precautions (5.1)] the following other adverse reactions associated with percutaneous transluminal septal myocardial ablation with the use of dehydrated alcohol, such as ablysinol, were identified in the literature: ventricular tachycardia and ventricular fibrillation. adverse reactions include arrhythmias, including ventricular tachycardia and/or ventricular fibrillation. ( 6 ) to report suspected adverse reactions, contact belcher pharmaceuticals at (727) 471-0850 or fda at 1-800-fda-1088 or www.fda.gov/medwatch.

Use in Specific Population:

8 use in specific populations ablysinol is not recommended during pregnancy. maternal use is not expected to result in fetal exposure to the drug. ( 8.1 ) the rate of heart blocks and dysrhythmia increased with age. (8.5) see 17 for patient counseling information 8.1 pregnancy risk summary the concentrations of alcohol in blood after ptsma were not measured, but ablysinol is not expected to increase significantly the systemic concentrations of endogenous alcohol following administration into a septal artery during percutaneous transluminal septal myocardial ablation. maternal use is not expected to result in fetal exposure to the drug. clinical considerations ablysinol for percutaneous transluminal septal myocardial ablation has not been evaluated in pregnant women and is not recommended during pregnancy. when possible, the percutaneous transluminal septal myocardial ablation procedure should be postponed in women until the postpartum period. data animal reproduction studies have shown
an adverse effect on the fetus and chronic fetal alcohol exposure is known to cause developmental defects in human. the developmental effects of acute ethanol exposure, such as from percutaneous transluminal septal myocardial ablation, have not been studied in pregnant or lactating women. 8.2 lactation ablysinol is not expected to increase significantly the systemic concentrations of endogenous alcohol following administration into a septal artery during percutaneous transluminal septal myocardial ablation and breastfeeding is not expected to result in exposure of the child to the drug. 8.4 pediatric use safety and effectiveness in pediatric patients have not been established. 8.5 geriatric use a comparison of the outcomes in patients with hypertrophic obstructive cardiomyopathy in patients < 60 years old and in patients ≥ 60 years old showed similar improvement in exercise capacity after ablation. the rate of heart blocks and dysrhythmia increased with age. permanent pacemaker dependency increased to 34% in patients > 60 years old.

Use in Pregnancy:

8.1 pregnancy risk summary the concentrations of alcohol in blood after ptsma were not measured, but ablysinol is not expected to increase significantly the systemic concentrations of endogenous alcohol following administration into a septal artery during percutaneous transluminal septal myocardial ablation. maternal use is not expected to result in fetal exposure to the drug. clinical considerations ablysinol for percutaneous transluminal septal myocardial ablation has not been evaluated in pregnant women and is not recommended during pregnancy. when possible, the percutaneous transluminal septal myocardial ablation procedure should be postponed in women until the postpartum period. data animal reproduction studies have shown an adverse effect on the fetus and chronic fetal alcohol exposure is known to cause developmental defects in human. the developmental effects of acute ethanol exposure, such as from percutaneous transluminal septal myocardial ablation, have not been studied in pr
egnant or lactating women.

Pediatric Use:

8.4 pediatric use safety and effectiveness in pediatric patients have not been established.

Geriatric Use:

8.5 geriatric use a comparison of the outcomes in patients with hypertrophic obstructive cardiomyopathy in patients < 60 years old and in patients ≥ 60 years old showed similar improvement in exercise capacity after ablation. the rate of heart blocks and dysrhythmia increased with age. permanent pacemaker dependency increased to 34% in patients > 60 years old.

Overdosage:

10 overdosage there is a direct correlation between the volume of alcohol and size of iatrogenic myocardial infarction. stop the procedure if there is failure to reduce the left ventricular outflow tract pressure gradient to less than 10 mmhg when reaching a total dose of 5 ml.

Description:

11 description ablysinol (dehydrated alcohol) injection is a sterile, preservative free solution of ≥ 99% by volume ethyl alcohol and no excipients. ablysinol is for cardiac septal branch intra-arterial use. it has a molecular formula of c 2 h 6 o and a molecular weight of 46.07. dehydrated alcohol injection, usp is a potent tissue toxin. ethanol is a clear, colorless, volatile, and flammable liquid miscible with water. it has the following structural formula: chemicalstructure

Clinical Pharmacology:

12 clinical pharmacology 12.1 mechanism of action dehydrated alcohol is a tissue toxin that produces a myocardial infarction when injected through an intra-arterial catheter into a target septal vessel, which causes the hypertrophied septum to thin. 12.2 pharmacodynamics a dose independent, approximate 70% reduction of the peak pressure gradient across left ventricular outflow tract is observed after injection of alcohol volumes in the range of 1-4 ml. remodeling contributes about 20% to the 70% total reduction in peak pressure gradient across the left ventricular outflow tract measured 12 months after septal ablation. other markers, such as infarct size or peak concentration of creatine kinase-mb (ck-mb), in contrast to peak pressure gradient across the left ventricular outflow tract, vary in proportion to the injected alcohol volume in the 1-4 ml range. 12.3 pharmacokinetics because injection of ablysinol during septal ablation is not expected to increase the systemic concentrations
of endogenous alcohol significantly, the pharmacokinetics of dehydrated alcohol are not expected to be clinically significant.

Mechanism of Action:

12.1 mechanism of action dehydrated alcohol is a tissue toxin that produces a myocardial infarction when injected through an intra-arterial catheter into a target septal vessel, which causes the hypertrophied septum to thin.

Pharmacodynamics:

12.2 pharmacodynamics a dose independent, approximate 70% reduction of the peak pressure gradient across left ventricular outflow tract is observed after injection of alcohol volumes in the range of 1-4 ml. remodeling contributes about 20% to the 70% total reduction in peak pressure gradient across the left ventricular outflow tract measured 12 months after septal ablation. other markers, such as infarct size or peak concentration of creatine kinase-mb (ck-mb), in contrast to peak pressure gradient across the left ventricular outflow tract, vary in proportion to the injected alcohol volume in the 1-4 ml range.

Pharmacokinetics:

12.3 pharmacokinetics because injection of ablysinol during septal ablation is not expected to increase the systemic concentrations of endogenous alcohol significantly, the pharmacokinetics of dehydrated alcohol are not expected to be clinically significant.

Nonclinical Toxicology:

13 nonclinical toxicology 13.1 carcinogenesis, mutagenesis, impairment of fertility ethanol (of alcohol beverages) was added to group 1 international agency for research on cancer (iarc) carcinogenicity ratings (iarc monographs). substances in this group are either carcinogenic to humans, or there is sufficient evidence of carcinogenicity in experimental animals and strong evidence in exposed humans that the substance acts through a relevant mechanism of carcinogenicity. alcohol consumption has been associated with various cancers, including liver, esophageal, breast, prostate, and colorectal cancer. since ablysinol is not expected to reach the systemic circulation following administration into a septal artery during percutaneous transluminal septal myocardial ablation, the recommended clinical use of the drug product is not expected to have carcinogenic risk in patients. literature reports suggest that ethanol is not mutagenic in the in vitro bacterial reverse mutation (ames) assay or
in vitro chromosomal aberration assays. ethanol is metabolized to acetaldehyde, which is a known mutagen. there are no data from either animal or human studies regarding potential for the impairment of fertility. 13.2 animal toxicology and/or pharmacology the median lethal dose (ld 50 ) values for ethyl alcohol given by intravenous and oral routes are 1440 and 7060 mg/kg in rats and 1973 and 3450 mg/kg in mice, respectively. the ld 50 for ethyl alcohol given by subcutaneous injection is 8285 mg/kg in mice.

Carcinogenesis and Mutagenesis and Impairment of Fertility:

13.1 carcinogenesis, mutagenesis, impairment of fertility ethanol (of alcohol beverages) was added to group 1 international agency for research on cancer (iarc) carcinogenicity ratings (iarc monographs). substances in this group are either carcinogenic to humans, or there is sufficient evidence of carcinogenicity in experimental animals and strong evidence in exposed humans that the substance acts through a relevant mechanism of carcinogenicity. alcohol consumption has been associated with various cancers, including liver, esophageal, breast, prostate, and colorectal cancer. since ablysinol is not expected to reach the systemic circulation following administration into a septal artery during percutaneous transluminal septal myocardial ablation, the recommended clinical use of the drug product is not expected to have carcinogenic risk in patients. literature reports suggest that ethanol is not mutagenic in the in vitro bacterial reverse mutation (ames) assay or in vitro chromosomal aber
ration assays. ethanol is metabolized to acetaldehyde, which is a known mutagen. there are no data from either animal or human studies regarding potential for the impairment of fertility.

Clinical Studies:

14 clinical studies evidence of the effectiveness of ethanol on exercise capacity in adults with symptomatic hypertrophic obstructive cardiomyopathy who are not candidates for surgical myectomy was obtained from literature involving over 4000 patients.

How Supplied:

16 how supplied/storage and handling ablysinol (dehydrated alcohol) injection is a clear, colorless liquid supplied in clear, glass, single-dose ampules. each ml contains ≥99% by volume ethyl alcohol. ndc volume single ampule carton of 10 ampules 1 ml 54288-105-01 54288-105-10 5 ml 54288-105-02 54288-105-15 store at room temperature, between 20°c and 25°c (68°f and 77°f). do not refrigerate or freeze. highly flammable, store away from any heat source.

Package Label Principal Display Panel:

Principal display panel - 1 ml ablysinol® (dehydrated alcohol injection, usp) 1 ml ndc 54288-105-01 for cardiac septal branch intra-arterial use. usual dose: see prescribing information. store away from any heat source. each ml contains: ≥ 99% by volume ethyl alcohol (a sterile, preservative free solution) warning: do not use if discolored or precipitated. 10 single dose ampules x 1 ml highly flammable rx only lot exp rev.r-1806 ablysinol1ml

Principal display panel - 5 ml ablysinol® (dehydrated alcohol injection, usp) 5 ml ndc 54288-105-02 for cardiac septal branch intra-arterial use. usual dose: see prescribing information. store away from any heat source. each ml contains: ≥ 99% by volume ethyl alcohol (a sterile, preservative free solution) warning: do not use if discolored or precipitated. 10 single dose ampules x 5 ml highly flammable rx only lot exp rev. r-1806 ablysinol5ml

Principal display panel - 5 ml carton ablysinol® (dehydrated alcohol injection, usp) 5 ml ndc 54288-105-15 for cardiac septal branch intra-arterial use. usual dose: see prescribing information. store away from any heat source. each ml contains: ≥ 99% by volume ethyl alcohol (a sterile, preservative free solution) warning: do not use if discolored or precipitated. 10 single dose ampules x 5 ml highly flammable rx only lot exp rev. r-1806 ablysinol5mlcover


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