Jubilant Pharmova Limited (JUBLPHARMA) — Announcement | 23 August 2026
Jubilant Pharmova announced that its USFDA-approved contract manufacturing facility in Spokane, USA, received approval for commercial batch production on Line 3, enabling sterile injectable and ophthalmic product launches in regulated markets. This milestone strengthens its contract manufacturing revenue streams and global pharma partnerships.
About Jubilant Pharmova Limited (JUBLPHARMA)
Healthcare · Pharmaceuticals · Listed on NSE
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📊 More JUBLPHARMA filings
- 🔴 Announcement — 1 September 2026 Jubilant Pharmova received a GST show cause notice from Mysore tax authorities on August 31, 2026, d...
- 🔴 Announcement — 28 August 2026 Jubilant Pharmova disclosed receipt of a GST show cause notice from the Joint Commissioner of CGST, ...
- 🟡 Board Meeting — 26 August 2026 Jubilant Pharmova held its 48th AGM on August 26, 2026, via video conference, passing all resolution...
- 🟡 Board Meeting — 10 August 2026 Jubilant Pharmova's board approved unaudited standalone and consolidated financial results for Q1 FY...
- 🔴 Financial Results — 10 August 2026 Jubilant Pharmova reported Q1 FY27 revenue of **₹2,229 crores**, up 17% YoY, driven by 19% growth in...
🔥 Also filed on 23 August 2026
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