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Drug companies can manufacture products under various brand names
Ramesh Shankar, Mumbai | Tuesday, October 30, 2012, 08:00 Hrs  [IST]

The confusion over the Union health ministry's recent directions to the state drug licensing authorities to grant or renew drug licences in proper generic names only is finally over. It has been finally clarified that the approval for drugs will henceforth be granted by the drug authorities only under generic names and the manufacturer can manufacture the product under various brand names.

Though persistent efforts to contact drug controller general of India (DCGI) Dr G N Singh for a clarification on the issue did not bear fruit, senior drug officials said that there is no ban on the use of brand names and the manufacturers can continue to affix their own brand names after getting the approval for their drugs in generic names from the state licensing authorities (SLAs). But, the brand names will not have the approval from the SLAs.

Presently, at the time of grant of the licence for manufacture of a drug formulation, the trade name as submitted by the manufacturer is also endorsed by the SLAs along with the generic name of the product thereby giving legitimacy to market the drug under the brand or the trade name. In fact, brand name issue is a trade mark issue over which the SLAs have no control but they were providing some legitimacy till now even when the trade mark or brand name was clashing with another name.

The manufacturer was always responsible for trade mark but now, after the ministry's directive, the SLAs will stay clear of any involvement in it. Now, the manufacturers only have to intimate the various brand names under which they will be manufacturing the drugs.

The health ministry had recently issued a directive, under Section 33 (P) of Drugs and Cosmetics (D&C) Act, 1940, to health secretaries of all states and union territories in which the ministry had directed that henceforth grant or renewal of manufacturing licences of drug formulations should be in proper/generic names only. The directive, which is mandatory to be followed as it is issued under Section 33 (P) of D&C Act, had created confusion among the manufacturers over the use of brand names.

Comments

Pankaj Nov 18, 2012 10:50 PM
This needs more clarification as most of state drug authorities have stopped approving new mfg licenses for products.

Madhav Nov 5, 2012 1:04 AM
I knew it...seems like the companies have lobbied and have got their job done...It would have been one of the best reforms of our times and would have saved expenditure of so many poor peole, but seems like it is more important for the authorities and govt to keep pharma companies in profit than helping the poor..
Anil Kumar Tripathi Nov 3, 2012 7:22 PM
Very useful information to us


Thanks
mp singh Oct 31, 2012 4:15 PM
a big boost for generic medicines especially for JAN AUSHADHI STORES,some sort of win for AN AUSHADHI STORES,
Hariprasad C K Oct 31, 2012 9:03 AM
Yes This article has given better clarity on licensing.

The only concern is for contract manufacturing site if they taken one generic name licence can they manufacture Drug product with different brands to different customers.
Srinivasan Ramachandran Oct 31, 2012 7:55 AM
The Govt. should direct the prescribers to recamand the drugs to their patients in Generic names only. Let the consumers have their options to buy the best company medicine at an offeardable price.it a right of the consumer.
Raj Kumar Mehta Oct 30, 2012 4:49 PM
This is nice move to get the licence and we can make them in different brand names. It save time and money.

I have the confusion that if any one sample (any brand name) drawn from any where in India and supposed it is failed by the authority then how one can make same product in other brands name., as the product is cancelled by the authority.


Raj Kumar Mehta Oct 30, 2012 4:49 PM
This is nice move to get the licence and we can make them in different brand names. It save time and money.

I have the confusion that if any one sample (any brand name) drawn from any where in India and supposed it is failed by the authority then how one can make same product in other brands name., as the product is cancelled by the authority.


Manasi Waghmare Oct 30, 2012 2:57 PM
This is very nice move towards easing the licence procedure.

I have only doubt as to what will happen in case of similar Brand Names and will there be any objection.

Also it is mentioned that "the manufacturers only have to intimate the various brand names under which they will be manufacturing the drugs."....Whom have the manufacturers to inform....

Await your positive reply


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