Food and drug act Flashcards

1
Q

The Food and Drug Regulations are divided into seven parts. What are the seven parts?

A
Part A: Administration 
Part B: Food 
Part C: Drugs
Part D: Vitamins, Minerals, and Amino Acids
Part E: Cyclamate Sweeteners  
Part G: Controlled Drugs
Part J: Restricted Drugs
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2
Q

What nine pieces of information must be found on the Manufacturer’s label

A
  1. Brand Name
  2. Generic Name
  3. Dosage Form
  4. Number of units in container
  5. Lot Number
  6. Expiry Date
  7. List of Medicinal Ingredients
  8. DIN
  9. Symbol of legal status product
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3
Q

What is the correct format for an expiry date

A

Year/ month/ day

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4
Q

Does Canada allow advertising for drugs or devices as treatment or prevention of disorders and diseases

A

Yes

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5
Q

The prescription Drug list is a list of medications that contain what?

A

all medication that requires a prescription in Canada that do not fall under the controlled drug and substance act.

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6
Q

How long is a prescription for a prescription drug list drug good for before a pharmacy cannot fill it ?

A

1 year

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7
Q

How long is a refill for a prescription drug list good for?

A

18 months after the first fill

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8
Q

How long must prescription records be kept

A

2 years from the date of the last fill

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9
Q

Transferring a prescription is known as what?

A

Giving a copy

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10
Q

True or false: Vitamins and minerals are only found in the Food and drug act regulations Part D

A

false

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11
Q

The Prescription drug list is divided into two sections? what are they?

A

Human use and Veterinary use

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12
Q

What is Part G (controlled drug) part I?

A

Single entity controlled drugs such as Ritalin

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13
Q

What is Part G (controlled drug) part II

A

Single entity controlled drugs such as Barbiturates

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14
Q

What is Part G (controlled drug) Part III

A

Anabolic Steroids

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15
Q

What is Part G (controlled drugs) Preparation

A

A combination product containing one controlled drug and one or more on-controlled drugs in therapeutic dose

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16
Q

What is the main thing that the NAPRA responsible for when a new drug comes out

A

Determining if the new drug is schedule I, II, III