Tainan City, Taiwan, July 17, 2018 — Handa Pharmaceuticals, Inc. (Taiwan Exchange: 6620) (“Handa”), summons an investor meeting to present the following information to institutional investors. “Handa is pleased to announce the rollout of its unique and creative ONCORE® drug delivery technology platform” applicable to the development of 505 (b)(2) new drugs, said Bill Liu,...Read More

Tainan City, Taiwan, June 6, 2017 — Handa Pharmaceuticals, Inc. (Taiwan Exchange: 6620) (together with its wholly owned U.S. subsidiary, Handa Pharmaceuticals, LLC, “Handa”), a specialty pharmaceutical company focusing on the research, development and commercialization of innovative prescription brand and high-barrier generic drug products, announced today that TruPharma, LLC (“TruPharma”) has started to market and...Read More

Tainan City, Taiwan, May 10, 2017 — Handa Pharmaceuticals, Inc. (Taiwan Exchange: 6620) (“Handa”), a specialty pharmaceutical company focusing on the research, development and commercialization of innovative prescription brand and high-barrier generic drug products, announced that its partner, Par Pharmaceutical, Inc. an Endo International company (“Par”), received final approval from the U.S. Food and Drug...Read More

Handa Pharmaceuticals. Inc. received the “Public Issuance” approval from Taiwan authorities on November 23th 2016. Stock ticker is 6620Read More

TAINAN TAIWAN, November 1, 2016 – Handa Pharmaceuticals, Inc. (“Handa”), a specialty pharmaceutical company based in Tainan, Taiwan, announced today that Par Pharmaceutical, Inc. (“Par”), an operating company of Endo International plc (NASDAQ: ENDP) (TSX: ENL) has begun shipping four dosage strengths (50 mg, 150 mg, 200 mg and 300 mg) of quetiapine fumarate extended...Read More

Pharmira Laboratories, Inc. completed the acquisition of US subsidiary Handa Pharmaceuticals, LLC., and its affiliate company Hangzhou Handa Pharmaceutical Technology Co. Ltd. in China.Read More

December 26, 2013 Handa Pharmaceuticals, LLC (“Handa”), a specialty pharmaceutical company based in Fremont, California, today announced that the U.S. Food and Drug Administration (“FDA”) has granted tentative approval of the Abbreviated New Drug Application (“ANDA”) for Dexlansoprazole Delayed Release Capsules, 60 mg, a generic version of Takeda’s DEXILANT®, which Handa transferred to Par Pharmaceutical,...Read More

October 29, 2012 Handa Pharmaceuticals, LLC (“Handa”), a specialty pharmaceutical company based in Fremont, California, today announced that it has entered into an exclusive acquisition and license agreement with Par Pharmaceutical, Inc. for Handa’s Abbreviated New Drug Application (“ANDA”) for quetiapine fumarate extended-release tablets, the generic version of AstraZeneca’s SEROQUEL XR®. Handa believes it is...Read More

April 19, 2012 Handa Pharmaceuticals, LLC (“Handa”), a specialty pharmaceutical company based in Fremont, California, today announced that it has entered into an exclusive acquisition and license agreement with Par Pharmaceutical, Inc. (NYSE: PRX) for Handa’s Abbreviated New Drug Application (“ANDA”) for Dexlansoprazole Delayed Release Capsules, a generic version of Takeda’s DEXILANT®. Handa believes that...Read More

October 3, 2011 Handa Pharmaceuticals, LLC (“Handa”), a specialty pharmaceutical company based in Fremont, California, today announced that it has reached an agreement with AstraZeneca to settle its U.S. patent litigation regarding Handa’s Abbreviated New Drug Application (“ANDA”) for Quetiapine Fumarate Extended-Release Tablets 50 mg., 150 mg., 200 mg., 300 mg., and 400 mg., a...Read More