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Zydus receives final approval from the USFDA for Balsalazide Disodium Capsules USP, 750 mg

Zydus Lifesciences Limited has received final approval from the United States Food and Drug Administration for Balsalazide Disodium Capsules USP, 750 mg.

Zydus announces Phase IV EVIDENCES-XI trial to generate Real World Evidence of Saroglitazar Mg in NAFLD patients with comorbidities

Zydus receives final approval from the USFDA for Esomeprazole Magnesium for Delayed-Release Oral Suspension, 20 mg and 40 mg

Zydus Lifesciences Limited has received final approval from the United States Food and Drug Administration for Esomeprazole Magnesium for Delayed-Release Oral Suspension, 20 mg and 40 mg.

Zydus receives final approval from the USFDA for Tadalafil Tablets USP, 20 mg

Zydus Lifesciences Limited has received final approval from the United States Food and Drug Administration for Tadalafil Tablets USP, 20 mg.

USFDA inspection at Zydus animal health drug manufacturing facility at SEZ, Ahmedabad

Zydus Lifesciences Ltd., today announced that the group s animal health drug manufacturing facility at SEZ, Ahmedabad underwent a USFDA inspection from 30th May to 2nd June, 2023. The inspection closed with nil observations.

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