Pharmaceutical Jurisprudence and Ethics Part I

The special law on counterfeit drug is known as RA__________

• 7394

• 3720

• 8203

• 5921

• NOTA (none of the above)

Based on the PNDF, the following are acting on the CNS except:

• Anti-gout

• Anti-schistosoma

• Anti-parkinsonism

• Anti-vertigo

It refers to the prevailing specified range of temperature, humidity, and other environment factors within optimal stability of the product:

• Storage conditions

• Temperature range

• Stability

• Expiry date

Requirement/s for registration of “Me-Too” or identical products includes:

• Toxicology data

• Pharmaceutical form of the drug

• Clinical evaluation data

• Mutagenicity

Government office where professionals register & where license is issued:

• PRC

• BFAD

• PPhA

• DDB

Equipment used for manufacturing, processing, packing, labeling, testing and control of drugs must be:

• Of suitable size

• Absorptive

• Impalpability

As defined in RA 8203, this refers to any entity, whether a single proprietorship, partnership, or corporation engaged in or doing business in the Philippines:

• residency

• business establishment

• brokering

• ownership

This refers to any facility used for the illegal manufacture of any dangerous drug/or controlled precursors and essential chemical.

• classrooms

• clandestine laboratory

• licensed establishment

• all of the above

Every prescription for external use filled in the drugstore shall bear a red label showing in black ink the components for such prescription and the word ______ at the bottom label:

• “Warning: May be habit-forming”

• “For External Use Only”

• “For Internal Use Only”

• “Flammable”

It refers to any establishments that imports raw material, active ingredients and finished products for its own use or for its own use or for distribution to other drug establishment or outlets:

• Exporter

• Importer

• Wholesaler

• Retailer