MSN Laboratories Gets CDSCO Panel Nod To Manufacture, Market Ferumoxytol Injection
Medically Reviewed By : Dr. Kamal Kant Kohli
Written By : Dr. Divya Colin
Published On 2024-07-10 12:30 GMT | Update On 2024-07-10 18:44 GMT
Advertisement
New Delhi: Accepting the pharmacokinetics study data and the published literature on global clinical trial data involving 112 Indian patients, the Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has approved the drug major MSN Laboratories to manufacture and market Ferumoxytol Injection 510 mg of elemental iron/17 mL (30 mg/ml).
However, this approval is subject to the condition that the firm conduct post-marketing surveillance (PMS) of the proposed drug.
Our comments section is governed by our Comments Policy . By posting comments at Medical Dialogues you automatically agree with our Comments Policy , Terms And Conditions and Privacy Policy .
Disclaimer: This website is primarily for healthcare professionals. The content here does not replace medical advice and should not be used as medical, diagnostic, endorsement, treatment, or prescription advice. Medical science evolves rapidly, and we strive to keep our information current. If you find any discrepancies, please contact us at corrections@medicaldialogues.in. Read our Correction Policy here. Nothing here should be used as a substitute for medical advice, diagnosis, or treatment. We do not endorse any healthcare advice that contradicts a physician's guidance. Use of this site is subject to our Terms of Use, Privacy Policy, and Advertisement Policy. For more details, read our Full Disclaimer here.
NOTE: Join us in combating medical misinformation. If you encounter a questionable health, medical, or medical education claim, email us at factcheck@medicaldialogues.in for evaluation.