LAWS AND ETHICS PART 2

Where do the three copies of Yellow Prescriptions go?

Has limited stock

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Forcing, coercing, or intimidating a duly registered and
licensed pharmacist to compound or dispense medical and
pharmaceutical products in violation of the provisions of

created a subcommittee on Food
and Drugs in the year 1961-62

was passed into law
--known as the “Food, Drug and Cosmetic Act”.

was appointed the first Director of the BFAD on Feb. 20, 1984 and took
her oath on Feb. 28, 1984.

On December 2, 1982, Executive Order No.
851 by Section 4, under the Minister of Health
Hon. Jesus M. Azurin, The FDA was abolished
and created the

FDA became BFAD under

In 1987, R.A. 3720 was amended by Executive Order 175 to the
new title

On 2009, BFAF is renamed again as

allow samples to be collected by the Food & Drug Administration or other appropriate government agency.

is known as the Generics Law of 1988.
It was signed into law on September 13, 1988.
By: Former Pres. Corazon Aquino

It is an act to promote, require,
and ensure the production of an
adequate supply, distribution, use,
and acceptance of drugs and
medicines identified by their
generic names.

(Labelling Requirement)

(Prescribing Requirement)

(Dispensing Requirement)

are used only to denote the set of
ethical principles perceived only by the professionals
themselves to be appropriate for their professional behavior.

in compounding and filling of
prescriptions and the dispensing of drugs, chemicals, and medicines

are demanded on the
part of those engaged in Pharmacy