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Alembic Pharmaceuticals Ltd Corporate Actions

1,041.85
(0.39%)
Nov 22, 2024|03:44:14 PM

CORPORATE ACTIONS

25/11/2023calendar-icon
24/11/2024calendar-icon

21 Jun 2024

12:00 AM

AGM

Announcement Date: 21 Jun, 2024

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18 Oct 2024

12:00 AM

Board Meeting

Agenda : Audited Result

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9 May 2024

12:00 AM

Dividend

Dividend Amount: 11

Record Date: 15 Jul, 2024

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Alembic Pharma: Related News

Alembic Pharma gets USFDA approval for generic heart failure medication
13 Nov 2024|09:20 AM

The authorised ANDA is a therapeutic equivalent of the reference-listed drug (RLD), Corlanor tablets, in the same 5 mg and 7.5 mg dosages.

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Alembic Pharma gets USFDA approval hypertension drug
11 Nov 2024|12:54 PM

These medications are also used to treat chronic stable angina and angina induced by coronary artery spasm.

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Alembic Pharma Gets USFDA Approval for Diltiazem ER Capsules
21 Oct 2024|12:26 PM

Alembic Pharmaceuticals continues to grow its footprint in the US, with this approval contributing to its robust portfolio of generic medications.

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Alembic Pharma's Gujarat plant clears USFDA inspection
9 Oct 2024|03:09 PM

The business stated that the authorised ANDA is therapeutically similar to the reference-listed drug product (RLD) Lastacaft Solution.

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Alembic Pharma Shares Jump on USFDA Approval for Lamotrigine Tablets
4 Oct 2024|10:39 AM

The approved Lamotrigine Extended-Release tablets are therapeutic equivalents of GlaxoSmithKline's Lamictal XR, with strengths of 200 mg, 250 mg, and 300 mg.

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Alembic Pharmaceuticals Gets US FDA Approval for Dabigatran Etexilate Capsules
13 Aug 2024|12:48 PM

Alembic Pharmaceuticals has got the final approval from USFDA for Dabigatran Etexilate Capsules, 110 mg.

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Alembic Pharma's Luphenazine Tablets Get USFDA Nod
25 Jul 2024|08:53 AM

Alembic has 210 ANDA approvals from the USFDA, including 182 final approvals and 28 tentative clearances.

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Alembic Pharma receives USFDA nod for generic Selexipag Injection
16 Jul 2024|03:08 PM

This certification allows a company to apply for approval of a generic drug before the patents of the brand-name drug expire.

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