"These products are not offered in countries where valid patents exist. However, final responsibility with respect to third party's patent rights in a specific country lies exclusively with the user."
 

ACTIVE PHARMACEUTICAL INGREDIENTS

  Atenolol USP
(US DMF No. 024024)
     
  Ciprofloxacin Hydrochloride USP
(U.S.DMF No. 17786)
     
  Cilnidipine
     
  Diclofenac Acid
(U.S.DMF No. 15366)
     
  Diclofenac Diethylamine BP
(US DMF No. 19020 & Spain DMF No. DD-708 / 01)
     
  Diclofenac Potassium BP/EP/USP
(Plant approved by FDA, U.S.A. - U.S.DMF No. 15074)
     
  Diclofenac Sodium BP/EP/USP
(U.S. DMF No 12469) (Spain DMF No. DS-092/978) (Canadian DMF No. 2005-055)
(Certicate of Suitability No. R1-CEP-1997-041-REV 03) .
     
  Diclofenac Sodium BP/EP/USP also Injectable Grade
     
  Gadopentatic Acid
     
  Nifedipine BP/EP/USP
(US DMF No. 16730)
(Certificate of Suitability No. RO-CEP 2000-096- REV. 02).
     
 
 
Products under development

• Cetrazine HCL

• Ofloxacin USP



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