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About 371 results for "food drug administration"

Zydus Cadila gets USFDA nod for blood pressure drug
Money Control

Zydus Cadila gets USFDA nod for blood pressure drug

The approval by the US Food and Drug Administration (USFDA) for diltiazem hydrochloride (Tiadylt ER) extended release capsules is for multiple strengths of 120mg, 180mg, 240mg, 300mg and 420mg, Cadila Healthcare said in a BSE filing. Money Control, 1 day ago
Zydus settles patent case over Aptalis' drug Canasa Business Standard, 3 days ago
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233 images for food drug administration

Money Control, 1 month ago
Sify, 2 months ago
Reuters, 2 months ago
Money Control, 1 month ago
Money Control, 1 month ago
Money Control, 1 month ago
Reuters, 3 months ago
Money Today, 2 months ago
Money Control, 2 months ago
DNA, 2 months ago
Money Control

Vivimed Labs zooms 8% on zero US FDA observations for Spain facility

After successful inspection, the US Food and Drug Administration has issued zero 483 observations for Spain facility.
 Money Control2 months ago Alkem Labs Taloja plant completes successful USFDA inspection  Business Standard1 month ago USFDA issues EIR for Granules India's Gagillapur plant  Business Standard1 day ago USFDA inspects Spain plant of Vivimed, no observations issued  Business Standard2 months ago
Money Control

Biocon tanks 9% after USFDA issues Form 483 with 10 observations to Bengaluru unit

The US Food and Drug Administration found lapses of current good manufacturing practices (cGMP) at company#39;s small molecule injectable plant in Bengaluru.
 Money Control1 week ago US FDA issues 5 observations for Lupin#39;s Pithampur Unit 3  Money Control1 month ago US FDA issued 3 observations to Srides Shasun#39;s Bangalore unit  Money Control2 months ago
Money Control

Lupin#39;s Aurangabad plant undergoes USFDA inspection

During the inspection, the US Food and Drug administration (USFDA) issued one 483 observation, Lupin said in a statement.
 Money Control2 weeks ago Lupin's Goa facility completes USFDA inspection  Business Standard3 weeks ago Torrent Pharma falls over 3.5% as US FDA issues 5 observations to Dahej plant  Money Control1 month ago Lupin may advance as Goa facility clears US FDA inspection  Business Standard3 weeks ago
DNA

FDA approves leukemia treatment developed by Celgene, Agios

(Reuters) - The U.S. Food and Drug Administration (FDA) on Tuesday approved Celgene Corp and Agios Pharmaceuticals Inc's oral treatment for acute myeloid leukemia (AML) patients with a rare genetic mutation.
 Reuters2 weeks ago FDA rejects Eagle Pharmaceuticals' heat stroke treatment  Reuters3 weeks ago Maharashtra FDA permits sale of pan masala  DNA3 weeks ago Aurobindo Pharma gains over 7.5% on US FDA nod to chronic kidney drug  Money Control4 weeks ago
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Sify

Expect EPS upgrades valuation rerating for Aurobindo: Surajit Pal

Aurobindo Pharma has gotten the United States Foods and Drug Administration (USFDA) approval for a generic drug that treats a chronic kidney disease. In an interview to CNBC-TV18, Surajit Pal of Prabhudas Lilladher spoke about the same.
 Money Control4 weeks ago Aurobindo Pharma shares end 4.5% higher on USFDA nod for drug  Business Standard4 weeks ago HDFC Securities expects Aurobindo Pharma to touch Rs 760  Money Control1 month ago Aurobindo receives USFDA approval to manufacture ADHD drug  Business Standard2 months ago
Money Control

Lupin launches generic conjunctivitis treatment medicine in US

The launch follows receipt of approval from the US Food and Drug Administration (USFDA) earlier for Moxifloxacin Hydrochloride Ophthalmic solution 0.5 per cent, the company said in a statement. The product is produced at Lupin#39;s Pithampur manufacturing ...
 Money Control1 month ago Lupin shares up nearly 4% on drug launch  Business Standard1 month ago Lupin launches generic skin cream in US  Business Standard1 month ago Lupin launches antidepressant tablets in US  Business Standard2 months ago
Money Control

Natco Pharma gets EIR from USFDA for Kothur unit

Natco Pharma announced the receipt of successful Establishment Inspection Report (EIR) from the US Food and Drug Administration (FDA) for the inspection conducted at its drug formulations facility at Kothur Unit, Telangana, India, during the period January ...
 Money Control4 weeks ago Natco Pharma receives EIR from USFDA, stock up 1.05%  Money Control4 weeks ago Pharmacovigilance unit of Ipca Laboratories receives EIR from US FDA: Sources  Money Control1 month ago Jeevan Scientific locked at 5% upper circuit on successful completion of USFDA audit  Money Control2 months ago
Money Control

Divis Labs zooms 20% as USFDA to lift import alert on unit-II at Visakhapatnam

The US Food and Drug Administration issued an import alert under clauses 99-32 and 66-40 in March of 2017.
 Money Control1 month ago Divi's Lab shares jump 20% in intra-day; later settles 8% up  Business Standard1 month ago USFDA to lift import alert on Visakhapatnam unit: Divi#39;s Labs  Money Control1 month ago Sensex Rises Over 245 Points; Divi's Lab Surges 7% as USFDA Lifts Import Alert  Equitymaster.com1 month ago
Money Control

Ban in US market due to change in drug shortage situation: Ipca labs

The company said its representatives got in touch with the US Food and Drug Administration (USFDA) to know the reasons behind the recent issuance of a warning letter to the company#39;s three plants at Pithampur, Silvassa, and Ratlam."
 Money Control1 month ago Ban in US mkt due to change in drug shortage situation: Ipca  Business Standard1 month ago Ipca Lab shares end over 8% lower as USFDA bans drug import  Business Standard2 months ago Ipca Labs tumbles over 15% as USFDA bans drug import  Business Standard2 months ago
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