Bepotastine Besilate

Product NDC
24208-630
11-digit product format
242080630
Labeler code
24208
Product ID
24208-630_995f4fe0-d861-4137-8090-a8ffc71c46f4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
bepotastine besilate
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Labeler
Bausch & Lomb Incorporated
Application
NDA022288
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2021-05-28
Substance
BEPOTASTINE BESILATE
Active strength
15 mg/mL
Pharmacologic classes
Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Orange Book products#

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
N022288-001BEPREVEBEPOTASTINE BESILATE1.5%SOLUTION/DROPS / OPHTHALMICATRLD, RS2009-09-08

Therapeutic equivalence codes#

Application-product, TE code table
Application-productTE code
N022288-001AT

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Bepotastine BesilateBEPOTASTINE BESILATEBausch & Lomb Incorporated995f4fe0-d861-4137-8090-a8ffc71c46f42020-12-31Warnings, Adverse reactionsExact identifier

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

warnings and cautions

5 WARNINGS AND PRECAUTIONS • Contamination of Solution: Do not touch the 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.

Adverse reactions cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

adverse reactions

6 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 Bausch & Lomb Incorporated at 1‑800-321-4576 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.

Additional Listing Data#

Finished product
Yes
Brand name base
Bepotastine Besilate
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BEPOTASTINE BESILATE15 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii6W18MO1QR3
Rxcui863038

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
79844758-4d97-abf0-31a3-9b38208d65a7Product name420250317

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
24208-630-05Bepotastine Besilate5 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS51
24208-630-05Bepotastine Besilate1 in 1 CARTONSOLUTION/ DROPS11
24208-630-10Bepotastine Besilate10 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS101
24208-630-10Bepotastine Besilate1 in 1 CARTONSOLUTION/ DROPS11

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
24208-630-05ML - Milliliter24208-6300912c035-6317-46e3-94a2-f9d4f02c76da12021-07-15
24208-630-10ML - Milliliter24208-6305b217ca1-da68-47c3-a8ca-75745150a0d912021-07-15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
24208-630BEPOTASTINE BESILATE SOLUTION/ DROPS [BAUSCH & LOMB INCORPORATED]1Current NDC, Legacy NDC, 4 package rows20210528_995f4fe0-d861-4137-8090-a8ffc71c46f4.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
863038bepotastine besilate 1.5 % Ophthalmic SolutionPSN995f4fe0-d861-4137-8090-a8ffc71c46f41
863038bepotastine besilate 15 MG/ML Ophthalmic SolutionSCD995f4fe0-d861-4137-8090-a8ffc71c46f41
863038bepotastine besilate 1.5 % Ophthalmic SolutionSY995f4fe0-d861-4137-8090-a8ffc71c46f41

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
24208-630-05242080630051 BOTTLE, DROPPER in 1 CARTON (24208-630-05) / 5 mL in 1 BOTTLE, DROPPER2021-05-280000-00-00NoNoCurrent
24208-630-10242080630101 BOTTLE, DROPPER in 1 CARTON (24208-630-10) / 10 mL in 1 BOTTLE, DROPPER2021-05-280000-00-00NoNoCurrent