Cadila's Aciloc Portfolio Faces Maharashtra FDA Action Over Similar Branding, Rs 2.45 Crore Stock Seized
Mumbai: The Maharashtra Food and Drug Administration (FDA) has barred the sale and distribution of some medicines manufactured by Cadila Pharmaceuticals Ltd and seized stock worth about Rs 2.45 crore across the state over branding similarities despite having different active pharmaceutical ingredients (APIs), officials said on Saturday.
The order is linked to Aciloc 150, Aciloc 150 Plus, Aciloc 300 and Aciloc 300 Plus, which have Ranitidine and Famotidine as APIs, they said.
He said compliance with norms governing branding, labelling and marketing of medicines must remain paramount to ensure patient safety.
In the statement, the FDA said it prohibited the sale and distribution of the available stock of the two medicines during inspections carried out on July 9 and 10 at the company's carrying and forwarding agent (CFA) warehouses in Pune, Nagpur as well as Bhiwandi in Thane district.The action covered medicine stock valued at Rs 2,45,37,490, it said.
"The company had earlier received approval to manufacture and market Aciloc 150 and Aciloc 300 containing active pharmaceutical ingredient Ranitidine. However, it later introduced Aciloc 150+ and Aciloc 300+, which contain Famotidine as active ingredient, while retaining almost identical branding and artwork except for the addition of the '+' symbol," it said.
According to the FDA, both the older Ranitidine-based medicines and the newer Famotidine-based variants were found to be available simultaneously in the market, creating the possibility of confusion among doctors, pharmacists and patients, and increasing the risk of dispensing or consuming the wrong medicine.
"Existing guidelines prohibit marketing medicines with a changed composition under substantially the same brand name. The preventive action was initiated to safeguard public health due to deceptive similarity in the brand names and the potential for patients to receive incorrect medication," it said.
The FDA said further investigation is underway and legal action will be taken under Drugs and Cosmetics Act 1940 and the rules framed under it based on the findings.
