Pharmaceutical company Dr Reddy's Laboratories Ltd (BSE:500124) (NSE:DRREDDY) (NYSE:RDY) on Monday announced the availability of the US Food and Drug Administration (USFDA) approved Ciprofloxacin 0.3% and Dexamethasone 0.1% Otic Suspension, USP.
According to the company, the Ciprofloxacin 0.3% and Dexamethasone 0.1% Otic Suspension, USP is available as 7.5 ml fill in a 10 ml bottle.
The company added that Dexamethasone 0.1% Otic Suspension, USP is the therapeutic equivalent generic version of Ciprodex (ciprofloxacin 0.3% and dexamethasone 0.1%) Otic Suspension. The Ciprodex brand had US sales of approximately USD453m MAT for the most recent 12 months ending in June 2020 according to IQVIA Health.
In addition, the company said its ciprodex is indicated for the treatment of infections caused by susceptible isolates of Acute Otitis Media in paediatric patients with tympanostomy tubes due to Staphylococcus aureus, Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis and Pseudomonas aeruginosa, as well as Acute Otitis Externa in paediatric, adult and elderly patients due to Staphylococcu.
Viatris names new chief legal officer
Alvotech signs biosimilar supply and commercialisation deals with Sandoz
InSysBio agrees new collaborative project with BeOne Medicines
MS Pharma enters strategic partnership with Hetero Group
Apiject to open new generic injectable drug manufacturing facility in Apex, NC
Bionpharma and STEERLife's Etravirine tablets approved by US FDA
ScinoPharm Taiwan secures first US FDA approval for complex multiple sclerosis generic
ScinoPharm Taiwan's Glatiramer Acetate Injection approved by US FDA
Accord Healthcare launches Clomiphene tablets in US market
Zentiva receives ESG Transparency Award 2025
Galmed Pharmaceuticals reports topline results for combination of Aramchol, Stivarga and metformin
Ingenus Pharmaceuticals' generic equivalent to Premarin receives US FDA approval
EirGenix signs second global exclusive licensing deal with Sandoz