Source: FDA, National Drug Code (US) Revision Year: 2019
BEPREVE (bepotastine besilate ophthalmic solution) 1.5% is a sterile, topically administered drug for ophthalmic use. Each mL of BEPREVE contains 15 mg bepotastine besilate. Bepotastine besilate is designated chemically as (+)4[[(S)-p-chloro-alpha-2-pyridylbenzyl]oxy]-1-piperidine butyric acid monobenzenesulfonate. The chemical structure for bepotastine besilate is:
Bepotastine besilate is a white to pale yellowish-white crystalline powder. The molecular weight of bepotastine besilate is 547.06 daltons. BEPREVE ophthalmic solution is supplied as a sterile, aqueous 1.5% solution, with an approximate pH of 6.8. The osmolality of BEPREVE (bepotastine besilate ophthalmic solution) 1.5% is approximately 295 mOsm/kg.
Each mL of BEPREVE (bepotastine besilate ophthalmic solution) 1.5% contains:
| Dosage Forms and Strengths |
|---|
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Ophthalmic solution containing bepotastine besilate 15 mg/mL (1.5%). |
| How Supplied |
|---|
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BEPREVE (bepotastine besilate ophthalmic solution) 1.5% is supplied in a white low density polyethylene bottle with a sterile linear low density polyethylene controlled dropper tip and a white polypropylene cap in the following sizes: NDC 24208-629-02 5 mL Bottle NDC 24208-629-01 10 mL Bottle |
| Drug | Countries | |
|---|---|---|
| BEPREVE | Canada, United States |
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