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Muthukrishnan

India

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Revision 2marks, 1 to 35


Revision 2marks, 1 to 35Version en ligne Finish this Quiz and post the screenshot in this group par Muthukrishnan 1 What is the Central Register under the Pharmacy Act, 1948? a A centralized list of pharmacists maintained by the Central Council. b A register of all pharmacies in India. c A database of drug prices maintained by the government. d A list of all medical practitioners in India. 2 Schedule H drugs can be dispensed only with what? a A general consent form. b A government permit for each sale. c An over-the-counter approval from a Pharmacist. d A prescription from a RMP. 3 Which statement correctly defines adulterated drugs? a Drugs degraded by contamination or insanitary manufacturing conditions. b Drugs sold without a prescription. c Drugs that are false claim, mixed with other branded drugs d Drugs with incorrect labeling and misleading 4 Ophthalmic preparations must include which label detail? Choose one or more answers a A proof of efficacy on label. b A sterility statement and preservation details. c No special labeling required. d For Ophthalmic use only 5 What is the DTAB in the Drugs and Cosmetics Act? a Drug Testing and Analysis Board. b Drugs Technical Advisory Board, the Act’s highest technical body. c Department of Therapeutic and Analytical Bioscience. d Drugs and Cosmetics Certification Agency. 6 What power does a Drug Inspector have under Section 22? a Only filing complaints. b Inspection, sampling, entering premises, and seizure. c Granting exemptions to imports. d Issuing licenses to manufacturers. 7 What does Misbranded cosmetics focus on? a The price control status of the product. b Only the packaging color used. c The drugs having highly contaminated and having toxic substances d False or misleading labeling and representations. 8 Who regulates Ayurvedic, Siddha, and Unani drugs under the Act? a Department of Traditional Medicine (DTM). b National Ayurvedic Regulatory Authority (NARA). c Central Bureau of Indian Standards (CBIS). d ASUDTAB (Ayurvedic, Siddha, Unani Drugs Technical Advisory Board). 9 What is the role of a Registered Medical Practitioner in drug regulation? a Inspects drug manufacturing sites. b Manufactures Schedule C and C1 drugs. c Prescribes Schedule H, H1, and X drugs; signs prescriptions. d Licenses retail pharmacies. 10 What is Schedule X primarily concerned with? a Highly addictive drugs. b Non-prescription analgesics. c Cosmetic ingredients only. d OTC vitamins and minerals. 11 What is the Central Register under the Pharmacy Act, 1948? a A centralized register of pharmacists maintained by the Central Council. b A government registry of pharmaceutical warehouses. c A list of approved drug formulas. d A register of medical practitioners in each state. 12 What is the main objective of Schedule H drugs? Choose one or more answers a Prevent self medications b Regulate the schedule H, C, C1, X drugs by use only with the prescription from the RMP'S c Over-the-counter sale allowed. d No prescription needed if brand is known. 13 Define adulterated drugs under the Act. a Drugs with incorrect labeling only. b Drugs manufactured outside India. c Drugs with expired shelf life only. d Drugs contaminated, prepared under unsanitary conditions, or containing deleterious substances. 14 What labeling is mandatory for ophthalmic preparations? Choose one or more answers a Name, concentration, sterility statements. b No label is required if in sealed vial. c Expiry date only is required. d , preservatives, and storage instructions. 15 Name the two main advisory bodies under the Drugs and Cosmetics Act. a DTAB and DCC. b CDL and IAS 16 What powers does a Drug Inspector have? Choose one or more answers a Inspect premises, b take samples, enter/search, c stop/search, and examine records. d Only inspect premises. 17 How is a drug deemed misbranded? a The drug is too expensive. b The bottle is too large. c Labeling or representation that is false or misleading. d Drug is manufactured outside India. 18 What are ASU drugs and who regulates them? a Herbal supplements with no regulation. b Ayurvedic, Siddha, Unani drugs regulated by ASUDTAB with standards in Schedule T. c Allopathic drugs regulated by DCGI only. d Cosmetics regulated by FDA. 19 Who is an RMP in these laws? a A pharmacist with PCI registration only. b Anyone with a medical background. c A nurse with medical training. d A practitioner registered in a medical register or eligible for registration. 20 What does Schedule X primarily regulate? a Highly addictive narcotics and psychotropic substances with strict controls. b All vaccines. c Topical antibiotics only. d Over-the-counter vitamins. 21 Differentiate Chemists and Druggists from Pharmacies. a Chemists dispense prescriptions; pharmacies sell only OTC. b Pharmacies sell only antibiotics. c Chemists/druggists sell ready-made medicines; pharmacies dispense and compound prescriptions. d Pharmacists are not required in pharmacies. 22 What is a manufacturing license type in the Act? a Export-only license. b Direct, Loan, and Repacking licenses. c Retail-only license. d Cosmetic-only license. 23 How are Schedule C and C1 different? a C1 is for injections; C is for tablets. b C is for cosmetics; C1 is for foods. c C is biological/special products (injections); C1 covers other special products needing control. d C1 is biological/special products (injections); C covers other special products needing control. 24 What defines a spurious drug? a Drug labeled in foreign language only. b Expired but usable drug. c Imitation or substitution, deceptive naming, or fictitious manufacturer details. d The drug not to be Imitation or substitution, deceptive naming, or fictitious manufacturer details. 25 What is Schedule G’s warning requirement? a Caution : Only the batch number is required. b Caution: dangerous to take without medical supervision. c No warning required. d Caution : Rx required on all Schedule G drugs. 26 What is DTAB’s role? Choose one or more answers a Only an auditing body. b guides policy and rule changes. c A licensing authority for retailers. d Highest technical advisory board; 27 What is the aim of DPCO 2013? a Price only based on manufacturer costs. b Market-based pricing to ensure affordable essential medicines. c Ban all price changes. d No price regulation for formulations. 28 What is the NLEM’s significance? a Unrelated to pricing. b Only a historical list with no current use. c Basis for price controls for essential medicines. d Used to ban imports only. 29 What is a Master Formula Record (MFR)? a A post-production audit report. b A marketing document. c A random note of batch numbers. d A blueprint for production including materials, steps, and controls. 30 What is Schedule P in the Act? a Import duty Schedule. b Advertising guidelines. c Life period and storage conditions for drugs. d Packaging design requirements. 31 What is a Restricted License? a A full pharmacy license. often where no pharmacist is present. b A license for medical devices only. c A license for exporting drugs only. d Retail sale license with limited drug categories, often where no pharmacist is present.

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Revision 2marks, 1 to 35Version en ligne

par Muthukrishnan

What is the Central Register under the Pharmacy Act, 1948?

Schedule H drugs can be dispensed only with what?

Which statement correctly defines adulterated drugs?

Ophthalmic preparations must include which label detail?

What is the DTAB in the Drugs and Cosmetics Act?

What power does a Drug Inspector have under Section 22?

What does Misbranded cosmetics focus on?

Who regulates Ayurvedic, Siddha, and Unani drugs under the Act?

What is the role of a Registered Medical Practitioner in drug regulation?

What is Schedule X primarily concerned with?

What is the Central Register under the Pharmacy Act, 1948?

What is the main objective of Schedule H drugs?

Define adulterated drugs under the Act.

What labeling is mandatory for ophthalmic preparations?

Name the two main advisory bodies under the Drugs and Cosmetics Act.

What powers does a Drug Inspector have?

How is a drug deemed misbranded?

What are ASU drugs and who regulates them?

Who is an RMP in these laws?

What does Schedule X primarily regulate?

Differentiate Chemists and Druggists from Pharmacies.

What is a manufacturing license type in the Act?

How are Schedule C and C1 different?

What defines a spurious drug?

What is Schedule G’s warning requirement?

What is DTAB’s role?

What is the aim of DPCO 2013?

What is the NLEM’s significance?

What is a Master Formula Record (MFR)?

What is Schedule P in the Act?

What is a Restricted License?