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7 ArticlesCADILAHC

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Cadila Healthcare US FDA Inspection of Baddi – Form 483 Revealed

Today we cover the Form 483 issued by the US FDA to Cadila Healthcare’s formulations manufacturing plant at Baddi. On another note, the company is due ...
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Amerisource Health Services Recalls 40 Lakh Antidepressant Tablets Manufactured By Cadila Healthcare

Based out of largest city in the US Columbus, Ohio – Amerisource Health Services (a subsidiary of AmerisourceBergen Corporation) – offers unit ...
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FDA’s New Rules Propels Generic and Biosimilar Approvals

Effective January 9th 2017, the US Food and Drug Administration (FDA) has announced an amendment to the final rule ((the rule governs the manner in which FDA ...
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Cadila Healthcare Recalls 14,808 Bottles of Capsules Used in The Treatment of Parkinson’s Disease

Cadila Healthcare – the 4th largest player in the Indian pharma market with 16 of the group’s brands feature amongst the top 300 pharma brands in India as ...
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Cadila Healthcare Recalls 2.2 Lakh Bottles of Venlafaxine Capsule

Cadila Healthcare – the 4th largest player in the Indian pharma market with 16 of the group’s brands feature amongst the top 300 pharma brands in ...
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Cadila Healthcare Gets Import Alert by WHO for Bad Manufacturing Practices

Cadila Healthcare was slapped with a World Health Organization (WHO) Notice of Concern (NOC) on the 29-Jan-15 (Note date: It’s three months ago) for the ...
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Premium: US FDA Warning Letter to Cadila Healthcare for Moraiya formulation facility and Ahmedabad API facility (Zyfine)

On the 23-Dec-15 (Wednesday), the US FDA issued a Warning Letter to Cadila Healthcare. The letter was in relation to the inspection performed from ...