Lupin Announces Approval from US FDA for Pitolisant Tablets
Lupin receives US Food and Drug Administration (FDA) approval for Pitolisant Tablets, 4.45 mg and 17.8 mg, a generic version of Wakix, for indications covered by the approved labeling.
Lupin Pharmaceuticals | 17/08/2026 | By News Bureau
Lupin Secures US Approval for Sodium Zirconium Cyclosilicate Oral Suspension
Lupin has received US Food and Drug Administration (FDA) approval for Sodium Zirconium Cyclosilicate Oral Suspension, 5 g and 10 g, bioequivalent to AstraZeneca’s Lokelma.
Lupin Pharmaceuticals | 11/08/2026 | By News Bureau
Lupin Launches Azilsartan Medoxomil Tablets in US
Lupin has launched Azilsartan Medoxomil Tablets in the US, a bioequivalent generic version of Edarbi, indicated for the treatment of hypertension in adults.
Lupin Pharmaceuticals | 17/06/2026 | By News Bureau | 117
US FDA Completes Pre-Approval Inspection at Lupin's Somerset Facility with One Observation
The US Food and Drug Administration (FDA) has completed a pre-approval inspection of Lupin’s manufacturing facility in Somerset, New Jersey, USA, with one observation.
Lupin Pharmaceuticals | 11/10/2025 | By Dineshwori | 584
Lupin Pharmaceuticals | 23/01/2023 | By Sudeep Soparkar | 1362
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