Manufacturer

The Production is done as per specification of  Master Formula Card (MFC), Batch Manufacturing Record (BMR) & Batch Packing Records (BPR) are maintained. All equipments are operated & cleaned as per (SOP’s.)  Deviations are minimized by adherence to above mentioned standards

All Equipments used for the manufacture are as per Good Manufacturing Practice and revised schedule -M.

All Non Sterile, Non ß Lactum & Non hormones formulations are currently made in our unit for Tablet, Sterile ß Lactum and Sterile Non ß Lactum formulations are currently made in this unit as Small Volume Parenteral. The construction for ß Lactum department on first floor.

All Equipments used for the manufacture are as per Good Manufacturing Practice and revised schedule -M.

We have following capacity for per month production based on single shift working.

Tablet                                                               100 lacs
Bolus                                                                  8 lacs
Small Volume (Liquid Injection)               8 lacs Vials
Powder Injection (ß Lactum)                     7 lacs vials

Adequate space as per GMP have been provided for the storage of raw & packing Materials , manufacturing , testing , in process controls etc.

Adequate measures have been taken to assure the quality of the products such as process & utility validations , proper sanitation, proper maintenance of equipments. All activities are performed by trained-skilled personnel and supervised by Competent personnel. Necessary records of all these are maintained.

Stability studies are carried out as per WHO guide lines. In the plant , GMP norms are followed. Measures are taken to prevent cross contamination.

Product Licensed to Manufacture

  • Uncoated, chewable, film coated, sugar coated, enteric coated, Tablets can be manufactured.
  • Small Volume Parenteral  ß Lactum  as well as  Non ß Lactum, are  manufactured  currently .

We also specialize in Non ß Lactum  tablets and bonus