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FDC gets USFDA’s nod for Cefixime for Oral Suspension

18 May 2026 Evaluate

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.

Peers
Company Name CMP
Sun Pharma. Inds. 1853.50
Dr. Reddys Labs. 1202.80
Cipla 1397.20
Lupin 2090.00
Zydus Lifesciences 1202.00
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