Major Export Products

Commodity

Chapter

30 - PHARMACEUTICAL PRODUCTS

Sub

3002 - Human blood; animal blood prepared for therapeutic, prophylactic or diagnostic uses; antisera, other blood fractions and immunological products, whether or not modified or obtained by means of biotechnological processes; vaccines, toxins, cultures of micr

Heading

300290 - Human blood; animal blood prepared for therapeutic, prophylactic or diagnostic uses; antisera, other blood fractions and immunological products, whether or not modified or obtained by means of biotechnological processes; vaccines, toxins, cultures of micr

Code

30029090 - Other Kits




Tariffs

Country Group Group Description Activity Tariff Rate Unit Valid From Valid To
ID-SAARC Import Duty - SAARC Countries Import 6 KGM 2016-01-01 9999-12-31
ID-OTHER Import Duty - Other Countries Import 10 KGM 2016-01-01 9999-12-31
TOT-INDIA Total Applicable Duty Rate - India Import 5 KGM 2016-01-01 9999-12-31
TOT-OSAARC Total Applicable Duty Rate - Other SAARC Countries Import 5 KGM 2016-01-01 9999-12-31
TOT-TIBET Total Applicable Duty Rate - Tibet Autonomous Region Import 5 KGM 2016-01-01 9999-12-31
TOT-OTHER Total Applicable Duty Rate - Others Import 5 KGM 2016-01-01 9999-12-31



Measures

Name Type Agency Description Comments Law Validity
Recommendation letter to be obtained for exportation or importation of drug Recommendation Requirement Ministry of Health To prevent the misuse or abuse of drugs and allied pharmaceutical substances and false or misleading information relating to the efficacy and use of drugs and to control the production, sale, distribution, export, import, storage and consumption of those drugs which are not safe for public consumption, efficacious and of standard quality Rupees 10 postage stamp in the application. Drug import and export fees as prescribed in Schedule-14. Drugs Registration Rules, 2038 (1981) 9999-12-31 00:00:00.0
Registration prior to importation of drug Registration Requirement Ministry of Health Prevent the misuse or abuse of drugs and alliedpharmaceutical substances and false or misleading information relating to the efficacy and use ofdrugs and to control the production, sale, distribution, export, import, storage and consumption ofthose drugs which are not safe for public consumption, efficacious and of standard quality. Rupees 10 Postage Stamp on the application formImport fees as per the Schedule 14 Drugs Registration Rules, 2038 (1981) 9999-12-31 00:00:00.0
Product license to be obtained to manufacture drug Licensing Requirement Ministry of Health Section 4- Product license to be obtained to manufacture drug Comments Drugs Registration Rules, 2038 (1981) 9999-12-31 00:00:00.0
Certificate of Origin Formality Requirement Ministry of Finance Section 21. Attachment of the documents with the declaration form: (1) A person importing or exporting goods pursuant to Section 18 of the Act, while submitting declaration form to the customs officer, shall submit the following documents including Certificate of Origin. Comments Customs Regulation, 2064 (2007) 9999-12-31 00:00:00.0
Generalized System of Preferences (GSP) Certificate Requirement Ministry of Finance 21. Attachment of the documents with the declaration form:(1) As per section 18 of the Act, the person importing or exporting goods,while submitting declaration form to the customs officer, should submitfollowing documents(a)..(b)...(c) For exportation(1) Invoice(2) Packing list(3) Certificate of Origin(4) Banking document regarding payment procedure, in case of export to third country(5) Documents which are required as per prevailing law regarding the recommendation, license, or certificate from any institution. However Certificate of Origin shall not be mandatory for the export in which G.S.P. certificate is required. Comments Customs Regulation, 2064 (2007) 9999-12-31 00:00:00.0



Procedures

Name Description Category View Procedure Detail with Relevant Forms
Recommendation letter to be obtained for exportation or importation of drug Aperson who intends to import or export a drug shall make an application to the Department. Rule 5. Procedure View
Registration prior to importation of drug Registration prior to importation of drug Procedure View
Certificate of Origin Procedure to apply for Certificate of Origin Procedure View