Commodity

Chapter

30 Pharmaceutical products

Heading

3003 Medicaments (excluding goods of heading 30.02, 30.05 or 30.06) consisting of two or more constituents which have been mixed together for therapeutic or prophylactic uses, not put up in measured doses or in forms or packings for retail sale.

Sub Heading

300331 - Other, containing hormones or other products of heading 29.37:

National Heading

30033100 -- Containing insulin

Tariffs

Displaying 1-8 of 8 result(s).

Country Group	Group Description	Activity	Tariff Rate	Unit	Valid From	Valid To
AP	Asia-Pacific TA - Import Duty	Import	Free	kg	30-06-2022	30-12-9999
IN	Indo-Sri Lanka FTA - Import Duty	Import	Free	kg	30-06-2022	30-12-9999
PK	Pakistan-Sri Lanka FTA - Import Duty	Import	Free	kg	30-06-2022	30-12-9999
SF	Agreement on South Asian Free Trade Area (SAFTA) - Import Duty	Import	Free	kg	30-06-2022	30-12-9999
SG	Singapore-Sri Lanka FTA	Import	Free	kg	30-06-2022	30-12-9999
GEN	Customs Duty	Import	Free	kg	30-06-2022	30-12-9999
VAT	Value Added Tax	Import	0%	kg	30-06-2022	30-12-9999
PAL	Port and Airport Development Levy	Import	0%	kg	30-06-2022	30-12-9999

Measures

Name	Type	Agency	Description	Comments	Law	Validity
General Import Control License	Licensing Requirement	Department of Import and Export Control	An import license is required for the importation of certain commodities, according to the Import and Export Control Act and its amendment. The import license is issued by the Department of Import and Export Control.	The import license requirement is applied to the importation of Insecticides and Pesticide substances, Non-Pesticides Chemicals, Chemicals, Petroleum Products & Lubricants, Radio Active Materials, Alcohol & Spirits, Live Animals & Animal Products, Corn & Maize and Cashew, Vehicles, Fish/Canned Fish, Tea, Explosives and Fire Arms, Coins, Sports Goods, Used Furniture,Sludge Oil , Metal Scraps and Waste, Plastic Food Containers, Western Drugs , Veterinary Medicine, Homoeopathic Drugs, Surgical Equipment,Industrial Chemicals, Mainly Ethyl alcohol (Ethanol) and Allied Products and Methanol Ethyl alcohol as an Ingredient for Alcohol, Perfumes and Allied Products, Other Industries and Laboratory Tests	Imports and Exports (Control) Act (Acts No. 1 of 1969; No. 48 of 1985; No. 28 of 1987)	31-12-9999

Procedures

Name	Description	Category	View Procedure Detail with Relevant Forms
General Import Control License	Department of Import and Export Control: Procedure for obtaining the General Import Control License	Import	View

Measures

Name	Type	Agency	Description	Comments	Law	Validity
Registration of a Drug	Registration Requirement	National Medicines Regulatory Authority	Standard Operating Procedure For Registration Of a drug	The basis for the regulatory control comes from the National Medicines Regulatory Authority Act, No. 5 Of 2015	National Medicines Regulatory Authority Act	31-12-9999

Procedures

Name	Description	Category	View Procedure Detail with Relevant Forms
The Registration of Drugs	Procedure to register Drugs	Import	View

Measures

Name	Type	Agency	Description	Comments	Law	Validity
Approval of a Company Profile	Licensing Requirement	National Medicines Regulatory Authority	Standard Operating Procedure For Registration Of Company Profiles	The company profile should be approved by NMRA	National Medicines Regulatory Authority Act	31-12-9999

Procedures

Name	Description	Category	View Procedure Detail with Relevant Forms
Registration Of Company Profiles(NMRA)	Procedure for Registration Of Company Profiles	Import	View

Measures

Name	Type	Agency	Description	Comments	Law	Validity
Import license for a Cosmetic, Device or a Drug	Licensing Requirement	National Medicines Regulatory Authority	Standard Operating Procedure For Import license for a Cosmetic, Device or a Drug	The basis for the regulatory control comes from the National Medicines Regulatory Authority Act, No. 5 Of 2015	National Medicines Regulatory Authority Act	31-12-9999

Procedures

Name	Description	Category	View Procedure Detail with Relevant Forms
The Import Licence for Drugs, medical Devices, Cosmetics	Procedure for obtaining The Import Licence for Drugs, medical Devices, Cosmetics	Import	View

Measures

Name	Type	Agency	Description	Comments	Law	Validity
Personal User Licence	Licensing Requirement	National Medicines Regulatory Authority	Standard Operating Procedure for Issuing Personal User Licence	The basis for the regulatory control comes from the National Medicines Regulatory Authority Act, No. 5 Of 2015	National Medicines Regulatory Authority Act	31-12-9999

Procedures

Name	Description	Category	View Procedure Detail with Relevant Forms
Personal User Licence(NMRA)	Procedure for obtaining The Personal User Licence	Import	View

Measures

Name	Type	Agency	Description	Comments	Law	Validity
License for Wholesale/Retail sale of Drugs	Licensing Requirement	National Medicines Regulatory Authority	Standard Operating Procedure For Issuing License for Wholesale/Retail sale of Drugs	The basis for the regulatory control comes from the National Medicines Regulatory Authority Act, No. 5 Of 2015	National Medicines Regulatory Authority Act	31-12-9999

Procedures

Name	Description	Category	View Procedure Detail with Relevant Forms
The Wholesale/Retail Licence (NMRA)	Procedure for Wholesale Licence	Import	View

Measures

Name	Type	Agency	Description	Comments	Law	Validity
The Sample Import Licence for Drugs, medical Devices, Cosmetics	Licensing Requirement	National Medicines Regulatory Authority	Procedure for obtaining The Sample Import Licence for Drugs, medical Devices, Cosmetics	The basis for the regulatory control comes from the Cosmetics, Devices and Drugs Act No. 27 of 1980.	National Medicines Regulatory Authority Act	08-12-9999

Procedures

Name	Description	Category	View Procedure Detail with Relevant Forms
The Sample Import Licence for Drugs, medical Devices, Cosmetics and Borderline products	Procedure for obtaining The Sample Import Licence for Drugs, medical Devices, Cosmetics,Borderline products	Import	View