SCHEDULE DII FORMAT.docVIP

SCHEDULE D (ll) (See rule 21 (d) and rule 24 A) Information required to be submitted by the manufacturer or his authorised agent with the Application Form for the registration of a bulk drug/formulation/special product for its import into India. The format shall be properly filled in and the detailed information, secret in future, may be furnished on a Computer Floppy. GENERAL Name of the drug/formulation/special product, a brief description and the therapeutic class to which it belongs. 1. Regulatory status of the drug. Free Sale Certificate and/or Certificate of Pharmaceutical Products