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Justice Court

HC quashes petition for selling Schedule H drug Sildenafil without license

The Karnataka High Court has quashed the criminal petition against Snapdeal, the New Delhi-based e-commerce company, for selling Schedule H drug Suhagra-100...
Rules Law Act

Drug Rules to include Liquid Antiseptic under Schedule K: Draft amendment

Download the notification: The ministry of health and family welfare has issued a draft amendment to include liquid antiseptics for household use...
NPPA Price of drugs

NPPA caps on trade margin of 42 Non Scheduled Cancer Drugs

Putting a cap on the trade margin of 42 select non-scheduled anti-cancer medicines by the National Pharmaceutical Pricing Authority (NPPA) resulted in reduction of up to...
Law Books Act

Schedules: All types of Drugs

Schedules –All types of Drugs under Drugs and Cosmetics Act 1940 and Rules 1945 Picture: Pixabay
Law Books Act

Schedules – Drugs and Cosmetics Act 1940 and Rules 1945

Schedules – Drugs and Cosmetics Act 1940 and Rules 1945 Picture: Pixabay As per...
Govt of India

Govt to include psoriasis drug acitretin in Schedule H

The Union health ministry will soon include psoriasis drug “Acitretin” in the Schedule H of the Drugs Rules, 1945 to prevent adverse...
Govt India

Govt outlines action plan for Schedule H & H1 drugs

Taking strong view of the fact that antimicrobial resistance (AMR) is increasingly becoming a serious threat to public health, the Union health...
Medicine

Hydroxychloroquine becomes a Schedule H1 drug

The Ministry of health through a special amendment categorised hydroxychloroquine (HCQS) drug as a schedule H1 drug- which means it cannot be sold over...
Medicine

1 Nation, 1 Molecule, 1 MRP for non scheduled drugs: MSME

The pharmaceutical micro small and medium enterprises (MSMEs) have urged the Department of Pharmaceuticals (DoP) to implement one nation, one molecule, one...
Medicine

A Schedule For OTC Drugs: NK Ahooja

A sub-committee, constituted by the Union Health Ministry to define the Over-the-Counter (OTC) drugs, has recommended to the government to classify the...
Law Books Act

Schedules: Drugs

Schedules: Drugs Schedules - drugs under Drugs and Cosmetics Act 1940 and Rules 1945
Govt of India

Govt notifies New Drugs and Clinical Trials (Amendment) Rules 2022

Download the notification: The Union health ministry has issued a final notification amending the New Drugs and Clinical Trials (ND&CT) Rules, 2019...
Laboratory

15 New Drugs to be developed: Sanofi

New Delhi: French drugmaker Sanofi SA (SASY.PA) will partner with British AI firm Exscientia Plc (EXAI.O) to develop up to 15 drug...
Rules Law Act

DTAB agrees to amend Rules for OTC drugs and license displaying in Medical Stores

The Drugs Technical Advisory Board (DTAB) has approved a proposal to amend the Drugs Rules to include a provision for the display...
Govt of India

Govt is expected to amend New Drugs and Clinical Trial Rules 2019

The government is expected to amend the New Drugs and Clinical Trial (ND & CT) Rules, 2019 to enable the manufacturing of...
Govt of India

Govt to allow parallel submission of these applications for New Drugs

The Drugs Technical Advisory Board (DTAB) has given its nod for the necessary amendment in the Drugs Rules for parallel submission of...
Medicine

Won’t allow drug peddlers to ruin lives of youth: HM

Haryana Health Minister Anil Vij on Sunday said that the Haryana State Narcotics Control Bureau (NCB) has been formed so that drug...
Drug recall

Drug recall: Torrent recalls 27,000 bottles of BP lowering drug

Torrent Pharma is recalling more than 27,000 bottles of its generic drug, used in lowering high blood pressure, in the US market.
USFDA

USFDA gives nod to Lupin for this drug to treat Kidney disease

Drug firm Lupin on Saturday said it has received approval from the US health regulator to market Sevelamer Carbonate for Oral Suspension, used in the control of...
Molecule Hormone Medicine

Benzene should be avoided in the manufacturing process of drugs due to this reason

Benzene should be avoided in the manufacturing process of drugs The USFDA is evaluating the root cause of...
Opinion People meeting

CDSCO panel weighing risks and benefits of Covid drug Molnupiravir

Antiviral Covid-19 pills People in the know said that Molnupiravir, which received emergency use authorisation (EUA) from the USFDA on Thursday, is likely...
Medicine Injection drug vaccine Syringe

Remdesivir drug should only be used in patients with ‘moderate to severe’ COVID-19: HM

The Centre on Friday said Remdesivir drug should only be used in patients with 'moderate to severe' COVID-19 and those with no...
Meeting Committee FDA

Schedule for 19 FDCs permitted pre-1988 to give online presentation

The Expert Committee appointed to evaluate the fixed dose combinations (FDCs) permitted before 1988, has invited stakeholders related to 19 FDCs for...
FDA Officers

Recruitment of 87 Drug Inspectors put on hold in Maharashtra

Maharashtra: The Maharashtra Public Service Commission (MPSC) has put the notification for the selection of 87 drug inspectors in the food and...

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