Ajanta Pharma Q4 PAT down 17% at Rs 94 cr

New Delhi: Ajanta Pharma on Wednesday reported 17.13 per cent decline in profit after tax (PAT)at Rs 94.49 crore for the quarter ended March 31, 2018 impacted by decline in institutional business in Africa.

The company had posted PAT of Rs 114.02 crore in January-March 2016-17, Ajanta Pharma said in a BSE filing.

Revenue from operations stood at Rs 530.31 crore in the quarter under review. It was at Rs 476.81 crore in the year-ago period.

Ajanta Pharma said revenue from operations were not comparable over previous year due to implementation of GST from July 1 last year as sales have been recorded as net of GST whereas earlier sales were recorded gross of excise duty which formed part of expenses.

Ajanta Pharma Managing Director Yogesh Agrawal said:”During the quarter, we have performed well in the Africa branded generic space. Whereas branded generic business in India and Asia performed below our expectations.”

There was a lot of movement in the Africa institution business that saw de-growth of 22 per cent which has impacted the overall quarter performance, he added.

“Considering the challenging pricing environment in the US, we have performed much better relative to our competitors who have seen much sharper price erosion,” Agrawal said.

For 2017-18, the company said, its PAT was at Rs 468.64 crore as compared to Rs 506.83 crore in 2016-17.

Revenue from operations was at Rs 2,130.86 crore as against Rs 2,001.64 crore in 2016-17, a growth of 6.46 per cent.

“Going forward, we will continue to focus on the branded generic business in India and emerging markets,” Agrawal said.

The company said in India, its sales rose 6 per cent at Rs 148 crore in the fourth quarter, whereas for the full year the same were at Rs 629 crore at a growth of 2 per cent.

Export sales in March quarter were at Rs 348 crore, up 10 per cent. For the full year, exports were at 1,434 crore, posting a growth of 9 per cent.

  • Related Posts

    Aurobindo Pharma gains after receving USFDA nod for Glycerol Phenylbutyrate Oral Liquid

    Aurobindo Pharma announced that it has received final approval from the U.S. Food and Drug Administration (USFDA) to manufacture and market Glycerol Phenylbutyrate Oral Liquid, 1.1 grams per ml. The…

    Legal Loopholes Stall Crackdown On Interstate Fake Drug Rackets In India

    New Delhi: Serious legal gaps in the Drugs and Cosmetics Act, 1940, combined with acute shortages of manpower and infrastructure, continue to impede the Central Drugs Standard Control Organisation (CDSCO)…

    Leave a Reply

    Your email address will not be published. Required fields are marked *

    You Missed

    Aurobindo Pharma gains after receving USFDA nod for Glycerol Phenylbutyrate Oral Liquid

    Aurobindo Pharma gains after receving USFDA nod for Glycerol Phenylbutyrate Oral Liquid

    Legal Loopholes Stall Crackdown On Interstate Fake Drug Rackets In India

    Legal Loopholes Stall Crackdown On Interstate Fake Drug Rackets In India

    Patna HC Rules Phenothiazine & Promethazine Not Narcotic Or Psychotropic Substances Under NDPS Act

    Patna HC Rules Phenothiazine & Promethazine Not Narcotic Or Psychotropic Substances Under NDPS Act

    COMT Inhibitors May Fuel Gut Bacteria That Degrade Levodopa In Parkinson’s Patients

    COMT Inhibitors May Fuel Gut Bacteria That Degrade Levodopa In Parkinson’s Patients

    Delhi Crime Branch Seizes Huge Stock Of Expired Baby Food, Cosmetics; One Arrested

    Delhi Crime Branch Seizes Huge Stock Of Expired Baby Food, Cosmetics; One Arrested

    FDA Releases Draft Guidance To Validate Non-Animal Testing Methods (NAMs) In Drug Development

    FDA Releases Draft Guidance To Validate Non-Animal Testing Methods (NAMs) In Drug Development