FDC has received abbreviated new drug application (ANDA) approval from United States Food and Drug Administration (USFDA), for Cefixime for Oral Suspension USP, 100 mg / 5 mL and 200 mg/ 5 mL.
Earlier, the company had received ANDA approval from USFDA for Fluconazole Tablets USP, 50 mg, 100 mg, 150 mg and 200 mg.
FDC is among India’s leading fully integrated pharmaceutical companies.