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The Economic Times
Alembic Pharma gets USFDA nod for generic product
Alembic Pharmaceuticals has received approval from the USFDA to market Albendazole Tablets USP (200 mg), a generic drug for treating infections caused by worms. The tablets are equivalent to Impax Laboratories' Albenza and are used for conditions like parenchymal neurocysticercosis and cystic hydatid disease. Alembic Pharma shares rose 2.79% on Thursday.
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Thu, Sep 5, 2024
Business Standard
Alembic Pharma shares rise after USFDA drug approval; check details here
Shares of Alembic Pharmaceuticals soared up to 4.13 per cent at Rs 1,135 per share on the BSE
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Tue, Aug 27, 2024
The Economic Times
Alembic Pharma gets USFDA nod for generic drug
Alembic Pharmaceuticals has been granted final approval from the USFDA for its generic Betamethasone Valerate Foam, intended to treat moderate-to-severe psoriasis of the scalp. This medication is equivalent to Luxiq Foam by Norvium Bioscience. Alembic’s shares ended 0.97% lower at Rs 1,089.90 on the BSE.
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Mon, Aug 26, 2024
Business Standard
Here's why Alembic Pharma stock skyrocketed 12% on August 26; details here
The surge in Alembic Pharma share price came after the company announced that it has received US Food & Drug Administration (USFDA) final approval for Betamethasone Valerate Foam, 0.12 per cent.
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Mon, Aug 26, 2024
Business Standard
Alembic Pharma gets USFDA nod for Betamethasone Valerate Foam
Alembic Pharmaceuticals announced that it has received final approval from the US Food & Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) Betamethasone Valerate Foam.
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Sat, Aug 24, 2024
Business Standard
Alembic Pharmaceuticals receives USFDA approval for Betamethasone Valerate Foam
Alembic Pharmaceuticals has received final approval from the US Food & Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) Betamethasone Valerate Foam, 0.12%. The approved ANDA is therapeutically equivalent to the reference listed drug product (RLD), Luxiq Foam, 0.12%, of Norvium Bioscience, LLC (Norvium).
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Sat, Aug 24, 2024
The Economic Times
Alembic gets USFDA nod for generic medication
Alembic Pharmaceuticals announced approval from the USFDA to market Dabigatran Etexilate Capsules (110 mg) for deep vein thrombosis prophylaxis, equivalent to Pradaxa Capsules. The company now has 211 ANDA approvals. Shares closed 3.17% lower at Rs 1,076 on the BSE.
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Tue, Aug 13, 2024
Business Line
FDA approves Alembic’s psoriasis drug
Alembic’s psoriasis drug Acitretin has $21-million market size
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Wed, Aug 7, 2024
The Economic Times
Alembic Pharma gets USFDA nod for generic Bromfenac ophthalmic solution
Alembic Pharmaceuticals Ltd has obtained final approval from the US FDA for its generic Bromfenac ophthalmic solution, used to treat postoperative inflammation and pain after cataract surgery. The approved product is equivalent to Prolensa Ophthalmic Solution, with an estimated market size of USD 168 million.
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Wed, Jul 10, 2024
Business Standard
Alembic receives USFDA approval for Bromfenac Ophthalmic Solution
Bromfenac Ophthalmic Solution 0.07% is a nonsteroidal anti-inflammatory drug (NSAID) indicated for the treatment of postoperative inflammation and reduction of ocular pain in patients who have undergone cataract surgery.
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Tue, Jul 9, 2024
The Economic Times
Alembic Pharma gets USFDA nod for Dabigatran Etexilate capsules
Alembic Pharmaceuticals Ltd received final approval from the US health regulator for generic Dabigatran Etexilate capsules 75 mg and 150 mg to reduce stroke and blood clots in adults with a specific medical condition.
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Tue, Jun 18, 2024
The Economic Times
Alembic Pharma gets USFDA nod for generic injection to treat hereditary angioedema
The approval by the US Food & Drug Administration (USFDA) is for the Abbreviated New Drug Application (ANDA) for Icatibant injection of strengths 30 mg/3 mL (10 mg/mL) single-dose prefilled syringe, Alembic Pharmaceuticals said in a regulatory filing.
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Mon, Jun 17, 2024