| 產品介紹： | 符合GMP規(guī)范要求勝于中西藥粉提取液、片劑、丸劑等生產過程中篩分過濾 Products: Requirements ofthe GMP standardis better thanWesternpowderextract,tablets, pillsand otherscreening filterproduction process 原料 | 比重 | 網目 | 機型 | 處理能力 | 中藥粉 | 0．8 | 80 | DT-800-1S | 550kg/h | 中藥液 | 0．9 | 150 | DT-1000-1S | 3000 kg/h | 顆粒制劑 | 0．8 | 12 | DT-1000-1S | 2500 kg/h | 西藥粉 | 0．6 | 80 | DT-1200-1S | 400 kg/h | 醫(yī)藥中間體 | 0．6 | 120 | DT-1200-1S | 300 kg/h | 浸膏 | 1．1 | 325 | DT-1200-1S | 1100 kg/h | 醫(yī)藥品 | 0．7 | 20、80 | DT-800-2S | 800 kg/h | 口服液 | 1．0 | 250 | DT-1000-1S | 2000 kg/h |
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The proportion ofrawprocessing powermeshmodels Inpowder0.8 80 DT-800-1S 550kg / h Inliquid0.9 150 DT-1000-1S 3000 kg / h Granules0.8 12 DT-1000-1S 2500 kg / h Western medicinepowder0.6 80 DT-1200-1S 400 kg / h Pharmaceutical intermediates0.6 120 DT-1200-1S 300 kg / h Extract1.1 325 DT-1200-1S 1100 kg / h Pharmaceuticals0.7 20,80 DT-800-2S 800 kg / h Oral1.0 250 DT-1000-1S 2000 kg / h | 
