Label: MIOCHOL E- acetylcholine chloride kit

  • NDC Code(s): 24208-539-20
  • Packager: Bausch & Lomb Incorporated
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated May 10, 2017

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  • SPL UNCLASSIFIED SECTION

    (acetylcholine chloride
    intraocular solution)
    20 mg/2 mL (10 mg/mL)
    Sterile

    1:100 with Electrolyte Diluent
    Rx only

    FOR INTRAOCULAR
    USE ONLY

  • DESCRIPTION

    Miochol-E (acetylcholine chloride intraocular solution) is a parasympathomimetic preparation for intraocular use. It is packaged in a blister pack containing one vial and one diluent ampule. The vial contains 20 mg acetylcholine chloride and 56 mg mannitol. The accompanying ampule contains 2 mL of a modified diluent of calcium chloride dihydrate, magnesium chloride hexahydrate, potassium chloride, sodium acetate trihydrate, and sterile water for injection.

    The reconstituted liquid will be a sterile isotonic solution (275–330 milliosmoles/kg) containing 20 mg acetylcholine chloride (1:100 solution) and 2.8% mannitol. The pH range is 5.0–8.2. Mannitol is used in the process of lyophilizing acetylcholine chloride, and is not considered an active ingredient.

    The chemical name for acetylcholine chloride, C7H16ClNO2, is Ethanaminium, 2-(acetyloxy)-N,N,N-trimethyl-, chloride and is represented by the following chemical structure:

    acetylcholine chloride (structural formula)
  • CLINICAL PHARMACOLOGY

    Acetylcholine is a naturally occurring neurohormone which mediates nerve impulse transmission at all cholinergic sites involving somatic and autonomic nerves. After release from the nerve ending, acetylcholine is rapidly inactivated by the enzyme acetylcholinesterase by hydrolysis to acetic acid and choline.

    Direct application of acetylcholine to the iris will cause rapid miosis of short duration. Topical ocular instillation of acetylcholine to the intact eye causes no discernible response as cholinesterase destroys the molecule more rapidly than it can penetrate the cornea.

  • INDICATIONS AND USAGE

    To obtain miosis of the iris in seconds after delivery of the lens in cataract surgery, in penetrating keratoplasty, iridectomy, and other anterior segment surgery where rapid miosis may be required.

  • CONTRAINDICATIONS

    Miochol-E is contraindicated in persons with a known hypersensitivity to any component of this product.

  • WARNINGS

    DO NOT GAS STERILIZE. If blister or peelable backing is damaged or broken, sterility of the enclosed vial and ampule cannot be assured. Open under aseptic conditions only.

  • PRECAUTIONS

    General

    If miosis is to be obtained quickly with Miochol-E, anatomical hindrances to miosis, such as anterior or posterior synechiae, must be released, prior to administration of Miochol-E. During cataract surgery, use Miochol-E only after delivery of the lens.

    Aqueous solutions of acetylcholine chloride are unstable. Prepare solution immediately before use. Do not use solution which is not clear and colorless. Discard any solution that has not been used.

    Drug Interactions

    Although clinical studies with acetylcholine chloride and animal studies with acetylcholine or carbachol revealed no interference, and there is no known pharmacological basis for an interaction, there have been reports that acetylcholine chloride and carbachol have been ineffective when used in patients treated with topical nonsteroidal anti-inflammatory agents.

    Pediatric Use

    Safety and effectiveness in pediatric patients have not been established.

  • ADVERSE REACTIONS

    Infrequent cases of corneal edema, corneal clouding, and corneal decompensation have been reported with the use of intraocular acetylcholine.

    Adverse reactions have been reported rarely, which are indicative of systemic absorption. These include bradycardia, hypotension, flushing, breathing difficulties, and sweating.

    To report SUSPECTED ADVERSE REACTIONS, contact Bausch + Lomb, a division of Valeant Pharmaceuticals North America LLC at 1-800-321-4576 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

  • OVERDOSAGE

    Atropine sulfate (0.5 to 1 mg) should be given intramuscularly or intravenously and should be readily available to counteract possible overdosage. Epinephrine (0.1 to 1 mg subcutaneously) is also of value in overcoming severe cardiovascular or bronchoconstrictor responses.

  • DOSAGE AND ADMINISTRATION

    Miochol-E (acetylcholine chloride intraocular solution) is instilled into the anterior chamber before or after securing one or more sutures.

    Instillation should be gentle and parallel to the iris face and tangential to pupil border.

    If there are no mechanical hindrances, the pupil starts to constrict in seconds and the peripheral iris is drawn away from the angle of the anterior chamber. Any anatomical hindrance to miosis must be released to permit the desired effect of the drug. In most cases, 0.5 to 2 mL produces satisfactory miosis. Note that the syringe filter supplied with Miochol-E has a priming volume of 0.6 mL (approximately).

    In cataract surgery, use Miochol-E only after delivery of the lens.

    Aqueous solutions of acetylcholine chloride are unstable. Prepare solution immediately before use. Do not use solution that is not clear and colorless. Discard any solution that has not been used.

  • DIRECTIONS FOR PREPARING MIOCHOL™-E:

    STERILE UNLESS PACKAGE OPEN OR BROKEN

    1.
    Inspect the unopened blister, vial, and ampule to ensure that they are all intact. Peel open the blister under a sterile field. Maintain sterility of the outer containers of the vial and ampule during preparation of solution.
    2.
    Aseptically attach a sterile 18–20 gauge, beveled needle to the luer tip of a sterile disposable syringe with a twisting motion to assure a secure fit.
    3.
    Break open the ampule containing the diluent. The One Point Cut (OPC) ampule must be opened as follows: Hold the bottom part of the ampule with the thumb pointing to the colored dot. Grasp the top of the ampule with the other hand, positioning the thumb at the colored dot, and press back to break at the existing cut under the dot.
    4.
    Remove the needle protector and withdraw the diluent from the ampule into the syringe. Discard the ampule.
    5.
    Remove and discard the cap from the top of the vial.
    6.
    Insert the needle through the center of the vial stopper, and transfer the diluent from the syringe to the vial. Shake gently to dissolve the powder.
    7.
    Slowly withdraw the solution from the vial through the needle into the syringe. Discard the needle.
    8.
    Aseptically open the syringe filter pouch, and attach the filter onto the luer tip of the syringe with a twisting motion to assure a secure fit.
    9.
    Aseptically attach a sterile blunt tip irrigation cannula to the male luer of the filter prior to intraocular irrigation.

    Discard the filter appropriately after use.

    Do not reuse the syringe filter.

    Do not aspirate and inject through the same filter.

  • HOW SUPPLIED

    Miochol-E
    (acetylcholine chloride intraocular solution)............................NDC 24208-539-20

    One blister pack containing the following components:

    Vial of 20 mg acetylcholine chloride powder for intraocular solution
    Ampule of 2 mL diluent

    One 0.2 micron sterile filter

    Priming volume 0.6 mL (approximately)

    Storage

    Store at 4°-25°C (39°-77°F)

    KEEP FROM FREEZING

    KEEP OUT OF REACH OF CHILDREN

    Manufactured for:
    Bausch + Lomb, a division of
    Valeant Pharmaceuticals North America LLC
    Bridgewater, NJ 08807 USA

    Manufactured by:
    Sanofi S.p.A.
    Via Valcanello, 4
    03012 ANAGNI (FR)

    Miochol is a trademark of Bausch & Lomb Incorporated or its affiliates.

    ©Bausch & Lomb Incorporated

    Rev. 05/2017
    9214904
    AB53920              

  • PACKAGE/LABEL PRINCIPAL DISPLAY PANEL

    carton.jpg

    NDC 24208-539-20

    Miochol-E
    (acetylcholine chloride
    intraocular solution)

    20 mg/2 mL (10 mg/mL)

    Sterile

    1:100 with Electrolyte
    Diluent

    FOR INTRAOCULAR
    USE ONLY

    Rx Only

    Contents:
    One Blister Pack containing:
    -20mg vial
    -2 mL diluent ampule
    One 0.2 micron sterile filter

    BAUSCH + LOMB

  • INGREDIENTS AND APPEARANCE
    MIOCHOL E 
    acetylcholine chloride kit
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:24208-539
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:24208-539-201 in 1 BLISTER PACK; Type 0: Not a Combination Product09/22/1993
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 VIAL 2 mL
    Part 21 AMPULE 2 mL
    Part 1 of 2
    MIOCHOL E 
    acetylcholine chloride solution
    Product Information
    Route of AdministrationINTRAOCULAR
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETYLCHOLINE CHLORIDE (UNII: AF73293C2R) (ACETYLCHOLINE - UNII:N9YNS0M02X) ACETYLCHOLINE CHLORIDE20 mg  in 2 mL
    Inactive Ingredients
    Ingredient NameStrength
    MANNITOL (UNII: 3OWL53L36A) 56 mg  in 2 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    12 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02021309/22/1993
    Part 2 of 2
    DILUENT 
    diluent solution
    Product Information
    Route of AdministrationINTRAOCULAR
    Inactive Ingredients
    Ingredient NameStrength
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    SODIUM ACETATE (UNII: 4550K0SC9B)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    12 mL in 1 AMPULE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02021309/22/1993
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02021309/22/1993
    Labeler - Bausch & Lomb Incorporated (196603781)
    Establishment
    NameAddressID/FEIBusiness Operations
    Norvatis Pharma Stein AG488152505MANUFACTURE(24208-539)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sanofi S.p.A.338454274MANUFACTURE(24208-539) , PACK(24208-539)