Drug Facts
Composition & Profile
Identifiers & Packaging
16 HOW SUPPLIED/STORAGE AND HANDLING Bepotastine Besilate Ophthalmic Solution, 1.5% is a sterile, clear colorless to pale yellow solution practically free from particles. Each mL of bepotastine besilate ophthalmic solution contains 15 mg bepotastine besilate equivalent to 10.7 mg bepotastine. Bepotastine besilate ophthalmic solution, 1.5% is supplied as a 5 mL or 10 mL solution in a 5 mL or 10 mL three piece container, respectively, each consisting of a white opaque low density polyethylene container with a white opaque open nozzle and a white high density polyethylene cap. 5 mL fill NDC 0378-7055-35 carton of one bottle 10 mL fill NDC 0378-7055-67 carton of one bottle Store at 15° to 25°C (59° to 77°F).; PRINCIPAL DISPLAY PANEL – 1.5% NDC 0378-7055-35 Bepotastine Besilate Ophthalmic Solution 1.5% For Topical Application in the Eye. Rx only 5 mL Each mL contains: Active: bepotastine besilate 15 mg equivalent to 10.7 mg bepotastine. Preservative: benzalkonium chloride 0.005% Inactives: monobasic sodium phosphate dihydrate, sodium chloride, sodium hydroxide to adjust pH, and water for injection. Usual Dosage: Instill one drop into the affected eye(s) twice a day. See accompanying prescribing information. This product is sterile when manufactured and should be dispensed in the original unopened container. Instruct patient on precautions to avoid contamination. Keep this and all medication out of the reach of children. Store at 15° to 25°C (59° to 77°F). Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. Made in India MCR:705535:1C:R1 Mylan.com M.L. No.: KTK/28/357/2006 Bepotastine Besilate Ophthalmic Solution 1.5% Carton Label
- 16 HOW SUPPLIED/STORAGE AND HANDLING Bepotastine Besilate Ophthalmic Solution, 1.5% is a sterile, clear colorless to pale yellow solution practically free from particles. Each mL of bepotastine besilate ophthalmic solution contains 15 mg bepotastine besilate equivalent to 10.7 mg bepotastine. Bepotastine besilate ophthalmic solution, 1.5% is supplied as a 5 mL or 10 mL solution in a 5 mL or 10 mL three piece container, respectively, each consisting of a white opaque low density polyethylene container with a white opaque open nozzle and a white high density polyethylene cap. 5 mL fill NDC 0378-7055-35 carton of one bottle 10 mL fill NDC 0378-7055-67 carton of one bottle Store at 15° to 25°C (59° to 77°F).
- PRINCIPAL DISPLAY PANEL – 1.5% NDC 0378-7055-35 Bepotastine Besilate Ophthalmic Solution 1.5% For Topical Application in the Eye. Rx only 5 mL Each mL contains: Active: bepotastine besilate 15 mg equivalent to 10.7 mg bepotastine. Preservative: benzalkonium chloride 0.005% Inactives: monobasic sodium phosphate dihydrate, sodium chloride, sodium hydroxide to adjust pH, and water for injection. Usual Dosage: Instill one drop into the affected eye(s) twice a day. See accompanying prescribing information. This product is sterile when manufactured and should be dispensed in the original unopened container. Instruct patient on precautions to avoid contamination. Keep this and all medication out of the reach of children. Store at 15° to 25°C (59° to 77°F). Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. Made in India MCR:705535:1C:R1 Mylan.com M.L. No.: KTK/28/357/2006 Bepotastine Besilate Ophthalmic Solution 1.5% Carton Label
Overview
Bepotastine besilate ophthalmic solution, 1.5% is a sterile, topically administered drug for ophthalmic use. Each mL of bepotastine besilate ophthalmic solution contains 15 mg bepotastine besilate. Bepotastine besilate is designated chemically as 4-[(S)-(4-Chlorophenyl)-2-pyridinylmethoxy]-1-piperidinebutanoic acid, benzenesulfonate salt. The chemical structure for bepotastine besilate is: Bepotastine besilate is a white or creamish white crystalline powder. The molecular weight of bepotastine besilate is 547.06 daltons. Bepotastine besilate ophthalmic solution is supplied as a sterile, aqueous 1.5% solution, with a pH of 6.8. The osmolality of bepotastine besilate ophthalmic solution, 1.5% is approximately 290 mOsm/kg. Each mL of bepotastine besilate ophthalmic solution, 1.5% contains: • Active: bepotastine besilate 15 mg (equivalent to 10.7 mg bepotastine) • Preservative: benzalkonium chloride 0.005% • Inactives: monobasic sodium phosphate dihydrate, sodium chloride, sodium hydroxide to adjust pH, and water for injection. Bepotastine Besilate Structural Formula
Indications & Usage
Bepotastine besilate ophthalmic solution, 1.5% is a histamine H 1 receptor antagonist indicated for the treatment of itching associated with signs and symptoms of allergic conjunctivitis. Bepotastine besilate ophthalmic solution is a histamine H 1 receptor antagonist indicated for the treatment of itching associated with allergic conjunctivitis. ( 1 )
Dosage & Administration
Instill one drop of bepotastine besilate ophthalmic solution into the affected eye(s) twice a day. Remove contact lenses prior to instillation of bepotastine besilate ophthalmic solution. Instill one drop into the affected eye(s) twice a day. ( 2 ) Remove contact lenses prior to instillation of bepotastine besilate ophthalmic solution. ( 2 )
Warnings & Precautions
• Contamination of Solution: Do not touch dropper tip to any surface. Keep bottle tightly closed when not in use. ( 5.1 ) • Contact Lens Wear: Bepotastine besilate ophthalmic solution should not be used to treat contact lens-related irritation. ( 5.2 ) 5.1 Contamination of Tip and Solution To minimize contaminating the dropper tip and solution, advise the patient not to touch the eyelids or surrounding areas with the dropper tip of the bottle and to keep the bottle tightly closed when not in use. 5.2 Contact Lens Wear Bepotastine besilate ophthalmic solution should not be used to treat contact lens-related irritation. Bepotastine besilate ophthalmic solution should not be instilled while wearing contact lenses. Patient should remove contact lenses prior to instillation of bepotastine besilate ophthalmic solution, because benzalkonium chloride may be absorbed by soft contact lenses. Lenses may be reinserted after 10 minutes following administration of bepotastine besilate ophthalmic solution.
Contraindications
Bepotastine besilate ophthalmic solution is contraindicated in patients with a history of hypersensitivity reactions to bepotastine or any of the other ingredients [see Adverse Reactions (6.2) ] . Hypersensitivity to any component of this product. ( 4 )
Adverse Reactions
The most common adverse reaction occurring in approximately 25% of patients was a mild taste following instillation. Other adverse reactions which occurred in 2-5% of subjects were eye irritation, headache, and nasopharyngitis. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Mylan Pharmaceuticals Inc. at 1-877-446-3679 (1-877-4-INFO-RX) 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 clinical practice. The most common reported adverse reaction occurring in approximately 25% of subjects was a mild taste following instillation. Other adverse reactions occurring in 2-5% of subjects were eye irritation, headache, and nasopharyngitis. 6.2 Post-Marketing Experience Hypersensitivity reactions have been reported rarely during the post-marketing use of bepotastine besilate ophthalmic solution. Because these reactions are reported voluntarily from a population of unknown size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. The hypersensitivity reactions may include itching, body rash, and swelling of lips, tongue and/or throat.
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