Aurobindo Receives FDA Approval for Cephalexin For Oral Suspension USP, 125 mg/5 mL and 250 mg/5 mL
Published: June 09, 2026
East Windsor, N.J. – Aurobindo Pharma Limited has received final approval from U.S. Food and Drug Administration for its Abbreviated New Drug Application Cephalexin For Oral Suspension USP, 125 mg/5 mL and 250 mg/5 mL. Aurobindo Pharma’s Cephalexin For Oral Suspension, are an AB-rated generic equivalent to the reference listed drug (RLD), Keflex for Oral Suspension, manufactured by Pragma Pharmaceuticals, LLC.
Cephalexin For Oral Suspension are indicated for the treatment of:
- Respiratory Tract Infections
- Otitis Media
- Skin and Skin Structure Infections
- Bone Infections
- Genitourinary Tract Infections
