Watson Pharmaceuticals has announced that its subsidiary has commenced commercial shipment of its Omeprazole delayed-release capsules USP product in the 40mg strength from its Davie, Florida manufacturing facility.
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In conjunction with the launch, Watson has 180 days of marketing exclusivity for being the first to file an abbreviated new drug application containing a paragraph IV certification for the 40mg strength.
Watson’s Omeprazole is the generic equivalent to AstraZeneca’s Prilosec delayed-release capsules USP and is indicated for the short-term treatment of active duodenal ulcer.
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