Shanghai, China
Business Type:
Number of Employees:
Year of Establishment:
Management System Certification:
ISO 9001
Average Lead Time:
Peak season lead time: one month
Off season lead time: one month
OEM/ODM Service

Pill Making Machine, Pill Machine, Pill Making manufacturer / supplier in China, offering Gzpl-680 Double Sided High-Speed Pill Making Machine, High Efficiency Fluidized Bed Dry Machine, Semi-Automatic Big Bag Powder Filling Machine and so on.

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Supplier Homepage Products Tablet Press Machine Gzpl-680 Double Sided High-Speed Pill Making Machine

Gzpl-680 Double Sided High-Speed Pill Making Machine

Get Latest Price
Min. Order / Reference FOB Price
1 Set US $293,000/ Set
Port: Shanghai, China
Production Capacity: 758000tablets/H
Payment Terms: L/C, T/T, D/P, Western Union, Paypal, Money Gram
Type: Pharmaceutical Packaging Machinery
Finished Dosage Form: Tablet
Precision: High Precision
Certification: CE, GMP, ISO
Voltage: 380V
Computerized: Non-Computerized

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Basic Info

Model NO.: GZPL-680
Customized: Customized
Condition: New
Warranty: 1 Year
Model: Pg79
Rated Power: 14kw
Weight: 4800kg
Noise: Less Than 85 Dba
Max.Mian Compression Force: 100kn
Max. Tablet Thickness: 8.5mm
Max.Diameter: 11mm
Overall Dimension: 1860mm*1720mm*2060mm
Trademark: SPM
Transport Package: Standard Export Wooden Cases
Specification: GMP and FDA.
Origin: China
HS Code: 8479820090

Product Description

Basic Info.
Model NO.:GZPL-680
Type:Preparation Machinery
Finished Dosage Form:Tablet
Precision:High Precision
Certification:CE, GMP, ISO, SGS
Warranty:1 Year
Export Markets:Global
Product Description
GZPL-680 Series High Speed Tablet Press is developed independently and newly 
produced by SPM. With advanced design and control technology, it is in a 
leading position domestically; Making advantage of own intellectual property, 
the main performances reach the international level in compliance with requirement of GMP and FDA.

Design of GMP & FDA
Same main and precompression
Interchangeable turret
Control by servo motor
Electronic record and signature in compliance with FDA 21 CFR Part 11


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