Sec. 11. If under this section a pharmacist substitutes a generically equivalent drug product for a brand name drug product prescribed by a practitioner, the prescription container label must identify the brand name drug for which the substitution is made and the generic drug. The identification required under this subsection must take the form of the following statement on the drug container label, with the generic name and the brand name inserted on the blank lines:
"_____________ Generic for _____________".
[Pre-1993 Recodification Citation: 16-6-8.1-2(f).]
As added by P.L.2-1993, SEC.25. Amended by P.L.186-1993, SEC.1.
Structure Indiana Code
Article 42. Regulation of Food, Drugs, and Cosmetics
Chapter 22. Drugs: Generic Drugs
16-42-22-4. "Generically Equivalent Drug Product"
16-42-22-5.5. Limitation of Effect of Chapter
16-42-22-6. Prescription Forms
16-42-22-8. Requirements for Substitution
16-42-22-9. Transmission of Practitioner's Instructions to Pharmacist
16-42-22-10. Substitution Prohibited
16-42-22-11. Substitution of Generic Drugs; Identification of Brand Name Drug
16-42-22-12. Identification of Manufacturer or Distributor of Dispensed Drug Product on Prescription