NDPS and related Flashcards
International law governing the control of drugs is composed primarily of UN conventions:
zz The Single Convention on Narcotic Drugs of 1961 (as amended in 1972)
zz Convention on Psychotropic Substances of 1971
zz United Nations Convention against illicit traffic in Narcotic Drugs and Psycho- tropic Substances of 1988.
National Policy on Narcotic Drugs and Psychotropic Substances is based on
on the directive Principles, contained in Article 47 of the Indian Constitution, which direct the State to endeavor to bring about prohibition of the consumption, except for medicinal purposes, of intoxicating drugs injurious to health.
Narcotic Drugs and Psychotropic Substances (NDPS) Act YEAR AND AMMENDMENTS
Narcotic Drugs and Psychotropic Substances (NDPS) Act 1985
Act was amended once in 1989 and subsequently in 2001 and 2014
Addict
means a person who has dependence on any narcotic drug or psychotropic substance
Narcotic drug
eans coca leaf, cannabis (hemp), opium, poppy straw and includes all manufactured drugs
‘’Psychotropic substance”
means any substance, natural or synthetic, or any natural material or any salt or preparation of such substance or material included in the list of psychotropic substances specified in the Schedule
Controlled substance”
means any substance which the Central Government may, having regard to the available information as to its possible use in the production or manufacture of narcotic drugs or psychotropic substances or to the provisions of any International Convention, by notification in the Official Gazette, declare to be a controlled substance
“Cannabis (hemp)” means-
Charas, Ganja and Any mixture of two.
Act excludes Bhang, Alcohol and Nicotine
“Licenced chemist” means
a person who has obtained a licence to possess, sell, exhibit or offer for sale or distribution by retail, essential narcotic drugs
“Licenced dealer”
means a person who has obtained a licence to possess, sell, exhibit or offer for sale or distribution by wholesale, essential narcotic drugs
“Essential narcotic drugs’’
the opioids identified for medical use (pain relief or OST, approved by the Drug Controller General of India. includes - Morphine, Methadone, Codeine, Hydrocodone, Oxycodone, and Fentanyl (which central government can notify on the basis of expediency in medical practice).
Offence and penalties under NDPS Act.
non bailable and non cognisable
SMALL, COMMERCIAL QUANTITY
amphetamine: 2g, 50 g
BPN : 2G, 20G
CHARAS/ HASHISH: 20G, 500 G
COCAINE: 1 KG, 20 KG
GANJA 5 G, 250 G
MDMS 0.5 G, 10 G
METHAMPETHAMINE 2G, 50 G
MORPHINE 5 G, 250 G
POPPY STAW 1KG , 50 KG
Punishment:
For small quantity 1 year rigorous imprisonment or a fine up to ` 10,000 or Both.
For commercial quantity: 5–10 years rigorous imprisonment or a fine of 1–2 lac or Both
zz Buprenorphine is a ——-
zz Methadone is a ——
zz Buprenorphine is a ‘’psychotropic’’
zz Methadone is a ‘’Narcotic’’
Guidelines for Stocking and Dispensing Essential Narcotic Drugs in Medical Institutions as per NDPS Act
Narcotic of relevance to deaddiction psychiatry practice: Methadone, Tramadol.
Background of problem statement: In India, despite need of opioids for good palliative care and opioid substitution therapy, use is not much preferred by health professionals. Complicated rules and regulations along with problems related to attitude and knowledge regarding pain relief and opioids substitution therapy among medical professionals and public are major hindrances for poor access to opioids.
The Amended NDPS Act 2014
zz Expanded the scope of the Act to include Medical and Scientific Use
zz Prepared a notified list of Essential Narcotic Drugs [ENDs], i.e. the opioids identified for medical use, approved by the Drug Controller General of India.
zz The notified list of ENDs currently includes - Morphine, Methadone, Codeine, Hydrocodone, Oxycodone, Tramadol and Fentanyl
zz It defined ‘Recognized Medical Institutions’ (RMIs) with criteria for stocking and
dispensing opioids for medical use.
zz Conferred the powers for authorizing medical institutions as RMIs, for stocking and
dispensing ENDs, to a single state agency - the State Drug Controller-SDC/Commissioner,
Food & Drug Administration-FDA
zz Those Institutions fulfilling the criteria to be RMIs, may apply to the State Drug Controller-
SDC/Commissioner, Food and Drug Administration - FDA, to procure and dispense ENDs. zz The authorization of RMIs is for periods of 3 years, and renewable from the same agency.