CYCLOSPORINE CYCLOSPORINE SAPTALIS PHARMACEUTICALS, LLC FDA Approved D ESCRIPTION Cyclosporine ophthalmic emulsion, 0.05% contains a topical calcineurin inhibitor immunosuppressant with anti-inflammatory effects. Cyclosporine’s chemical name is Cyclo[[(E)-(2S,3R,4R)-3-hydroxy-4-methyl-2-(methylamino)-6-octenoyl]-L-2-aminobutyryl-N-methylglycyl-N-methyl-L-leucyl-L-valyl-N-methyl-L-leucyl-L-alanyl-D-alanyl-N-methyl-L-leucyl-N-methyl-L-leucyl-N-methyl-L-valyl] and it has the following structure: Structural Formula Formula: C 62 H 111 N 11 O 12 Mol. Wt.: 1202.6 Cyclosporine, USP is a white or almost white powder. Cyclosporine ophthalmic emulsion appears as a white opaque to slightly translucent homogeneous emulsion. It has an osmolality of 230 to 320 mOsmol/kg and a pH of 6.5-8.0. Each mL of cyclosporine ophthalmic emulsion contains: Active: cyclosporine, USP 0.05%. Inactives: carbomer copolymer type A; castor oil; glycerin; polysorbate 80; sodium hydroxide to adjust pH; and water for injection. image description
FunFoxMeds bottle
Substance Cyclosporine
Route
OPHTHALMIC
Applications
ANDA211943

Drug Facts

Composition & Profile

Dosage Forms
Drops
Strengths
0.5 mg/ml 0.4 ml 0.9 ml
Quantities
4 ml 9 ml 5 vial 30 vial 60 vial
Treats Conditions
1 In Dications And Usage Cyclosporine Ophthalmic Emulsion Is Indicated To Increase Tear Production In Patients Whose Tear Production Is Presumed To Be Suppressed Due To Ocular Inflammation Associated With Keratoconjunctivitis Sicca Increased Tear Production Was Not Seen In Patients Currently Taking Topical Anti Inflammatory Drugs Or Using Punctal Plugs Cyclosporine Is A Calcineurin Inhibitor Immunosuppressant Indicated To Increase Tear Production In Patients Whose Tear Production Is Presumed To Be Suppressed Due To Ocular Inflammation Associated With Keratoconjunctivitis Sicca Increased Tear Production Was Not Seen In Patients Currently Taking Topical Anti Inflammatory Drugs Or Using Punctal Plugs 1

Identifiers & Packaging

Container Type BOTTLE
UNII
83HN0GTJ6D
Packaging

16 H OW SUPPLIED /S TORAGE AND H ANDLING Cyclosporine ophthalmic emulsion is packaged in sterile, preservative-free single-dose vials. Each vial contains 0.4 mL fill in a 0.9 mL LDPE vial; 5 vials are packaged in an aluminum pouch; 6 or 12 such pouches are placed in a carton. The entire contents of each carton (30 vials and 60 vials) must be dispensed intact. 30 Vials 0.4 mL each - NDC 71656-012-30 60 Vials 0.4 mL each - NDC 71656-012-60 Storage: Store at 20° to 25 °C (68° to 77 °F), with excursions permitted between 15° to 30°C (59° to 86°F) [See USP Controlled Room Temperature].; Package/Label Display Panel NDC 71656-012-30 cycloSPORINE Ophthalmic Emulsion 0.05% Sterile, Preservative-Free Rx only 30 Single-Dose Vials (0.4 mL each) 30; Package/Label Display Panel NDC 71656-012-60 cycloSPORINE Ophthalmic Emulsion 0.05% Sterile, Preservative-Free Rx only 60 Single-Dose Vials (0.4 mL each) Vials-60

Package Descriptions
  • 16 H OW SUPPLIED /S TORAGE AND H ANDLING Cyclosporine ophthalmic emulsion is packaged in sterile, preservative-free single-dose vials. Each vial contains 0.4 mL fill in a 0.9 mL LDPE vial; 5 vials are packaged in an aluminum pouch; 6 or 12 such pouches are placed in a carton. The entire contents of each carton (30 vials and 60 vials) must be dispensed intact. 30 Vials 0.4 mL each - NDC 71656-012-30 60 Vials 0.4 mL each - NDC 71656-012-60 Storage: Store at 20° to 25 °C (68° to 77 °F), with excursions permitted between 15° to 30°C (59° to 86°F) [See USP Controlled Room Temperature].
  • Package/Label Display Panel NDC 71656-012-30 cycloSPORINE Ophthalmic Emulsion 0.05% Sterile, Preservative-Free Rx only 30 Single-Dose Vials (0.4 mL each) 30
  • Package/Label Display Panel NDC 71656-012-60 cycloSPORINE Ophthalmic Emulsion 0.05% Sterile, Preservative-Free Rx only 60 Single-Dose Vials (0.4 mL each) Vials-60

Overview

D ESCRIPTION Cyclosporine ophthalmic emulsion, 0.05% contains a topical calcineurin inhibitor immunosuppressant with anti-inflammatory effects. Cyclosporine’s chemical name is Cyclo[[(E)-(2S,3R,4R)-3-hydroxy-4-methyl-2-(methylamino)-6-octenoyl]-L-2-aminobutyryl-N-methylglycyl-N-methyl-L-leucyl-L-valyl-N-methyl-L-leucyl-L-alanyl-D-alanyl-N-methyl-L-leucyl-N-methyl-L-leucyl-N-methyl-L-valyl] and it has the following structure: Structural Formula Formula: C 62 H 111 N 11 O 12 Mol. Wt.: 1202.6 Cyclosporine, USP is a white or almost white powder. Cyclosporine ophthalmic emulsion appears as a white opaque to slightly translucent homogeneous emulsion. It has an osmolality of 230 to 320 mOsmol/kg and a pH of 6.5-8.0. Each mL of cyclosporine ophthalmic emulsion contains: Active: cyclosporine, USP 0.05%. Inactives: carbomer copolymer type A; castor oil; glycerin; polysorbate 80; sodium hydroxide to adjust pH; and water for injection. image description

Indications & Usage

IN DICATIONS AND USAGE Cyclosporine ophthalmic emulsion is indicated to increase tear production in patients whose tear production is presumed to be suppressed due to ocular inflammation associated with keratoconjunctivitis sicca. Increased tear production was not seen in patients currently taking topical anti-inflammatory drugs or using punctal plugs. Cyclosporine is a calcineurin inhibitor immunosuppressant indicated to increase tear production in patients whose tear production is presumed to be suppressed due to ocular inflammation associated with keratoconjunctivitis sicca. Increased tear production was not seen in patients currently taking topical anti-inflammatory drugs or using punctal plugs. ( 1 )

Dosage & Administration

D OSAGE AND ADMINISTRATION Invert the unit-dose vial a few times to obtain a uniform, white, opaque emulsion before using. Instill one drop of cyclosporine ophthalmic emulsion twice a day in each eye approximately 12 hours apart. Cyclosporine ophthalmic emulsion can be used concomitantly with lubricant eye drops, allowing a 15-minute interval between products. Discard vial immediately after use. Instill one drop of cyclosporine ophthalmic emulsion twice a day in each eye approximately 12 hours apart. ( 2 )

Warnings & Precautions
W ARNINGS AND P RECAUTIONS To avoid the potential for eye injury and contamination, be careful not to touch the vial tip to your eye or other surfaces. ( 5.1 ) 5. 1 Potential for Eye Injury and Contamination Be careful not to touch the vial tip to your eye or other surfaces to avoid potential for eye injury and contamination. 5.2 Use with Contact Lenses Cyclosporine ophthalmic emulsion should not be administered while wearing contact lenses. Patients with decreased tear production typically should not wear contact lenses. If contact lenses are worn, they should be removed prior to the administration of the emulsion. Lenses may be reinserted 15 minutes following administration of cyclosporine ophthalmic emulsion.
Contraindications

C ONTRAINDICATIONS Cyclosporine ophthalmic emulsion is contraindicated in patients with known or suspected hypersensitivity to any of the ingredients in the formulation. Hypersensitivity ( 4 )

Adverse Reactions

A DVERSE R EACTIONS The following serious adverse reactions are described elsewhere in the labeling: Potential for Eye Injury and Contamination [ see Warnings and Precautions ( 5.1 ) ] The most common adverse reaction following the use of cyclosporine ophthalmic emulsion was ocular burning (17%). ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Saptalis Pharmaceuticals, LLC at 1-833-727-8254 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. In clinical trials, the most common adverse reaction following the use of cyclosporine ophthalmic emulsion was ocular burning (17%). Other reactions reported in 1% to 5% of patients included conjunctival hyperemia, discharge, epiphora, eye pain, foreign body sensation, pruritus, stinging, and visual disturbance (most often blurring). 6.2 Post-marketing Experience The following adverse reactions have been identified during post-approval use of cyclosporine ophthalmic emulsion. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. Reported reactions have included: hypersensitivity (including eye swelling, urticaria, rare cases of severe angioedema, face swelling, tongue swelling, pharyngeal edema, and dyspnea); and superficial injury of the eye (from the vial tip touching the eye during administration).


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