Perrigo Company (Nasdaq: PRGO; TASE) announced today that the Hatch-Waxman litigation relating to Duac® Gel (clindamycin phosphate (1%) and benzoyl peroxide (5%) gel) filed by the Stiefel Laboratories division of Glaxo SmithKline has been dismissed with Perrigo Company has received final FDA approval for its abbreviated new drug application (ANDA) for clindamycin phosphate and benzoyl peroxide 1.2% / 5% topical gel, the generic equivalent of Duac gel. Duac Gel is indicated for the topical treatment of Patent litigation for this product was dismissed with prejudice in 2009. Perrigo has commenced shipment of the product. Duac gel (clindamycin phosphate and benzoyl peroxide 1.2 per cent / 5 per cent gel) is indicated for the topical treatment of Perrigo Company (Nasdaq: PRGO) announced that it has purchased the ANDA for clindamycin phosphate (1%) and benzoyl peroxide (5%) gel from KV Pharmaceutical for $14 million in cash at closing and a $2 million milestone payment upon the completion of a Perrigo Company has announced that it has purchased the ANDA forclindamycin phosphate (1 and benzoyl peroxide (5%) gel from KVPharmaceutical for $14 million in cash at closing and a $2 million milestonepayment upon the completion of a successful technical CONDITIONS OF USE: The information in this database is intended to supplement, not substitute for, the expertise and judgment of healthcare professionals. The information is not intended to cover all possible uses, directions, precautions, drug .
The detailed view includes drug products with safety labeling changes to the BOXED WARNING, CONTRAINDICATIONS, WARNINGS, PRECAUTIONS, ADVERSE REACTIONS, or PATIENT PACKAGE INSERT/MEDICATION GUIDE sections. Deletions or editorial revisions made to these Within this, 983 patients received the approved dose of umeclidinium 62.5mcg once-daily. Approval of Duac Combination Gel The MHLW also today announced the approval of Duac Combination Gel in Japan, for use in the treatment of acne vulgaris. Duac Perrigo Co. (PRGO) recently announced that it had received US Food and Drug Administration (:FDA) approval for its abbreviated new drug application (ANDA) for the generic version of Duac Gel. With the Perrigo ANDA being the first para IV filing In June, the company gained FDA approval for its abbreviated new drug application (ANDA) for its generic version of Duac Gel. Duac Gel, developed by Stiefel, a GlaxoSmithKline (GSK - Analyst Report) company, is a clindamycin phosphate and benzoyl peroxide .
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