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Anti-Rh(D) Immunoglobulin Injection

Anti-Rh(D) immunoglobulin injection is a blood fraction containing antibodies against the Rh(D) antigen, derived from human plasma. It is administered prophylactically to prevent hemolytic disease of the newborn in Rh-negative mothers. This product is classified under tariff item 3002.12.00 as an antiserum prepared for therapeutic use.

Import Duty Rates by Country of Origin

Origin CountryMFN TariffSurtaxesTotal Effective Rate
πŸ‡¨πŸ‡³ChinaFreeβ€”Free
πŸ‡²πŸ‡½MexicoFreeβ€”Free
πŸ‡ΊπŸ‡ΈUnited StatesFreeβ€”Free
πŸ‡©πŸ‡ͺGermanyFreeβ€”Free
πŸ‡―πŸ‡΅JapanFreeβ€”Free

Alternative Classifications

This product could be classified differently depending on its characteristics or intended use.

3006.30.00Same rate: Free

If the product is a diagnostic reagent for blood-grouping

Blood-grouping reagents are specifically classified under heading 30.06.

3002.14.00Same rate: Free

If the product is a monoclonal antibody rather than a polyclonal antiserum

Monoclonal antibodies are classified under subheading 3002.14.

Not sure which classification is right?

The Tariff Assistant works through the GRI rules on your specific product to reach the right tariff item β€” and can price the duty on it in the same conversation.

Import Tips & Compliance

β€’ Include the product monograph and proof of Health Canada approval for the therapeutic use

β€’ Ensure the product is packaged for retail sale or as a measured dose, which may affect classification

β€’ Verify that the product is not a diagnostic reagent, which would fall under heading 38.22

Related Products under Tariff item 3002.12.00

Botulinum Toxin Type A Immune Globulin

Botulinum toxin type A immune globulin is an antitoxin derived from human plasma fractions containing antibodies against botulinum toxin. It is used to treat infant botulism by neutralizing the toxin. This product falls under tariff item 3002.12.00 as an immunological blood fraction for therapeutic neutralization.

Botulism Antitoxin (Trivalent, Equine)

Botulism Antitoxin (Trivalent, Equine) is an antiserum derived from equine plasma containing antibodies that neutralize botulinum neurotoxins A, B, and E. It is used therapeutically for the treatment of botulism poisoning. This product falls under tariff item 3002.12.00 as an antiserum prepared for therapeutic uses.

Cryoprecipitated Antihemophilic Factor from Human Plasma

Cryoprecipitated Antihemophilic Factor from Human Plasma is a human plasma fraction rich in factor VIII, fibrinogen, and von Willebrand factor. It is prepared by thawing frozen plasma at 1-6Β°C and used to treat hemophilia A and fibrinogen deficiencies. This product falls under tariff item 3002.12.00 as a blood fraction for therapeutic use.

Cytomegalovirus (CMV) Hyperimmune Globulin

Cytomegalovirus (CMV) hyperimmune globulin is a plasma fraction enriched with CMV-specific antibodies, used to prevent CMV infection in transplant patients. It is prepared from pooled human plasma of donors with high antibody titers. This product is classified under tariff item 3002.12.00 as a blood fraction prepared for prophylactic use.

Cytomegalovirus Immune Globulin Intravenous (CMV-IGIV)

Cytomegalovirus Immune Globulin Intravenous (CMV-IGIV) is a purified immunoglobulin fraction derived from human plasma of donors with high CMV antibody titers. It is used prophylactically to prevent CMV infection in transplant patients. This product falls under tariff item 3002.12.00 as a blood fraction prepared for therapeutic or prophylactic uses.

Cytomegalovirus Immune Globulin Intravenous (CMV IGIV)

Cytomegalovirus Immune Globulin Intravenous (CMV IGIV) is a human immune serum containing high-titer antibodies against cytomegalovirus, used prophylactically in transplant patients. It falls under tariff item 3002.12.00 as human immune blood sera fractionated from pooled plasma.