Genix Pharmaceuticals Corporation announced that it has entered into an agreement with a regulatory consulting company to prepare and file Abbreviated New Drug Submissions (ANDS) with Health Canada for the first 10 of its 30 generic ophthalmic drugs, acquired by the company. An ANDS is an application to Health Canada to approve a prescription generic pharmaceutical for sale in Canada. Upon approval of an ANDS, Health Canada issues the applicant with a Marketing Authorization and Drug Identification Number (DIN), which allows the applicant to legally sell the drug in Canada. Upon submission of these ten ANDS applications, the Company expects to receive Health Canada approvals and issuance of these DINs within 12 months. Upon completion of the first ten ANDS filings, the company shall immediately proceed with the ANDS filings of the remaining twenty ophthalmic drugs in GENIX's portfolio.