The conformity evaluation of generic drugs entered the harvest period, and in May a large number of varieties were evaluated

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Pharmaceutical Network Industry Dynamic" statistics, up to now, 882 generic products through or as if through consistency evaluation, 167 product regulations have been evaluated more than two, 88 product regulations have been evaluated more than three ..The industry said that the consistency evaluation of generic drugs has entered the harvest period, many enterprises ushered in the consistency evaluation approval of the peakWith the eye coming to an end in May 2020, which varieties of pharmaceutical companies pass the generic consistency evaluation in May this year? The author did a partial combingShanghai Pharmaceuticals: Subsidiary Generic Drugs through consistency evaluation
May 29, Shanghai Pharmaceutical son-in-law Changzhou Pharmaceutical Co., Ltdreceived the State Drug Administration issued on the chlorine-nitrogen flat tablets of the "drug supplementary application approval" (lot number: 2020B03113), through the consistency evaluation of generic drugsit is understood that chlornitis tablets are mainly suitable for refractory schizophrenia, as early as 1972 in SwitzerlandIn May 2019, Changzhou Pharmaceuticals applied to the State Drug Administration for the consistent evaluation of generic drugs and accepted the applicationAs of the disclosure date, Changzhou Pharmaceuticals' consistent evaluation of the drug has been invested in research and development costs of about 7.61 million yuanAnti-Pharma: Amoxicillin Particles through the conformity evaluation of generic drugs
Lu anti-drug may 28 evening announcement, the company received the State Drug Administration issued on amoxicillin particles of the "drug supplementary application approval", the drug through the quality and efficacy consistency evaluation of generic drugsIn 2019, amoxicillin grain domestic sales of about 300 million yuan, the company's sales revenue of the product is 10.31 million yuanFosun Pharmaceuticals: Holding subsidiary drug bekaluamine tablets through the generic drug consistency evaluation
Fosun Pharmaceuticals issued a notice on the evening of May 26, recently, the company's holding subsidiary Shanghai Chaozhao Pharmaceutical Co., Ltd(hereinafter referred to as "Shanghai Chaozhao") received the State Drug Administration on the Picaluamine tablets issued by the Pharmaceutical Supplementapplication Application Approval (batch number: 2020B03039), the drug through the generic evaluation of the drugIt is reported that the picamine tablets are mainly suitable for the treatment of advanced prostate cancerZhendong Pharmaceuticals: Katopli tablets through the generic drug consistency evaluationZhendong Pharmaceuticals may 26 evening announcement, recently, the company's wholly-owned subsidiary Ant Bio, received the State Drug Administration approved the issuance of the Katopli tablets 25mg specifications of the "drug supplementary application approval", the drug through the quality and efficacy consistency evaluation of generic drugsCatopli tablets are competitive angiotensin-converting enzyme inhibitors, clinical indications for hypertension, heart failureEnhua Pharmaceuticals: Gabba spray capsules through the generic drug consistency evaluationEnhua Pharmaceuticals on the evening of May 20, the company recently received the State Drug Administration approved the issuance of the "drug supplementary application approval", the company's Gabba spray capsule through the quality and efficacy consistency evaluation of generic drugsGabba spit capsule indications: 1, nerve pain after herpes infection: for the treatment of post-herpes nerve pain in adults2Epilepsy: Auxiliary treatment for adults and children over 12 years of age with or without secondary systemic seizuresIt can also be used for complementary treatment of partial seizures in children between 3 and 12 years of ageHaizheng Pharmaceuticals: Do you take McCorcortholcecapsule capsules through the generic drug consistency evaluation
Haizheng Pharmaceuticals may 18 evening announcement, the company received the National Drug Administration approved the issuance of the "drug supplementary application approval" for McCorcorthin capsules, the company's cocorphenol capsules have passed the quality and efficacy consistency evaluation of generic drugs Is it suitable for organ rejection in patients receiving allogeneic kidney or liver transplants and should be used in conjunction with corticosteroids and cyclosporine or taquemotis Pro Pharmaceuticals: Amoxicillin capsules through the generic drug consistency evaluation
Pro Pharmaceutical Sina announcement, the company's wholly-owned subsidiary Zhejiang Jutai Pharmaceutical Co., Ltd received the State Drug Administration approved the issuance of the "drug supplementary application approval" on amoxicin capsules, the drug through the generic drug consistency evaluation Amoxicillin clinically is widely used to treat upper respiratory tract infections, urogenital tract infections, soft tissue infections, lower respiratory tract infections, and other drugs to eradicate Helicobacter pylori, and patients with mild and moderate kidney disease do not need to adjust their doses Amoxicillin capsules have been added to the Class A health insurance and the 2018 National Base Drug Catalog Guangji Pharmaceuticals: Vitamin B2 tablets through consistency evaluation
Guangji Pharmaceutical Sinaccord announcement, the company received the State Drug Administration approved the issuance of "vitamin B2 tablets" of the "drug supplementary application approval", the drug through the quality and efficacy of the drug consistency evaluation Vitamin B2 tablets are used to prevent and treat vitamin B2 deficiency, such as keratitis, dry lip, tongue inflammation, carclaves, conjunctivitis, seborrheic dermatitis, etc Xinhua Pharmaceuticals: Ibuprofen tablets (0.1g and 0.2g) through the generic drug consistency evaluation Xinhua Pharmaceuticals announced that the company received the Approval of Ibuprofen tablets (0.1g and 0.2g) approved by the State Drug Administration, the product through the quality and efficacy consistency evaluation of generic drugs ("generic drug consistency evaluation") The company became the first domestic ibuprofen tablet0.2g, 0.1g second through the product agency consistency evaluation of the drug ibuprofen tablets for heat relief analgesics, is a medical insurance Class A drug, used to relieve light to moderate pain such as headache, joint pain, migraine, toothache, muscle pain, nerve pain, pain, but also for the common cold or influenza-induced fever Ibuprofen is a children's anti-fever drug recommended by the World Health Organization and the U.S FDA Zhejiang sincere pharmaceutical industry: hydrochloric acid amino glucose capsules (three product regulations) through the conformity evaluation of generic drugs , Zhejiang Sincere Pharmaceutical Co., Ltd produced amino glucose capsules (three product regulations) through the generic drug consistency evaluation, the State Drug Administration issued the pharmaceutical supplementary application approval; The company became wenzhou's first pharmaceutical company to pass a generic consistency evaluation Treasure Island Pharmaceuticals: Metformin hydrochloride through consistency evaluation
May 11, Treasure Island announced that Harbin Treasure Pharmaceutical Co., Ltd., a wholly-owned subsidiary of Heilongjiang Treasure Island Pharmaceutical Co., Ltd., received the Approval of the State Drug Administration to issue the "drug supplementary application approval" approved by the State Drug Administration (0.25g), the product passed the quality and efficacy consistency evaluation of generic drugs To date, the Drug Enforcement Administration's Drug Review Center has accepted 39 applications for consistency evaluation of metformin hydrochloric acid tablets and approved 25 application numbers, including 21 metformin hydrochloride tablets (0.25g) and 4 metformin hydrochloride tablets (0.5g) Treasure Island is the second company in the Heilongjiang region to pass a consistency rating for this species (0.25g) Lisheng Pharmaceuticals: Bicarbonate tablets through the generic drug consistency evaluation Lisheng Pharmaceuticals May 6 noon announcement, the company recently received the State Drug Administration issued on the sodium bicarbonate tablets (hereinafter referred to as "the drug") 0.5g specifications of the "drug supplementary application approval", the drug through the quality and efficacy consistency evaluation of generic drugs Sodium bicarbonate adaptation is used to relieve stomach pain, heartburn (heartburn) and acid reflux caused by excessive stomach acid The company said the drug is helped to improve the competitiveness of the drug market by evaluating the quality and efficacy of generic drugs.