Centre has prohibited the exports of Injection Remdesivir and Remdesivir Active Pharmaceutical Ingredients (API) till the COVID situation in the country improves.
‘India is witnessing a recent surge in COVID cases. As on April 11, there are 11.08 lakh active COVID cases and they are steadily increasing. This has led to a sudden spike in demand for Injection Remdesivir used in treatment of COVID patients. There is a potential of further increase in this demand in the coming days,’ the Union Ministry of Health and Family Welfare said in a statement here on Sunday.
Seven Indian companies are producing Injection Remdesivir under voluntary licensing agreement with M/s Gilead Sciences, USA. They have an installed capacity of about 38.80 lakh units per month.
‘In light of the above, the Government has prohibited the exports of Injection Remdesivir and Remdesivir Active Pharmaceutical Ingredients (API) till the situation improves,’ the Ministry said.
In addition, the Government has taken the following steps to ensure easy access of hospital and patients to Remdesivir
All domestic manufactures of Remdesivir have been advised to display on their website, details of their stockists/distributors to facilitate access to the drug.
Drugs inspectors and other officers have been directed to verify stocks and check their malpractices and also take other effective actions to curb hoarding and black marketing.
The State Health Secretaries will review this with the Drug Inspectors of the respective States/UTs. The Department of Pharmaceuticals has been in contact with the domestic manufacturers to ramp up the production of Remdesivir.