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NDC Package Code : 12714-234
Start Marketing Date : 2000-06-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER, FOR SOLUTION (50mg/50mg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 12714-236
Start Marketing Date : 2000-06-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER, FOR SOLUTION (25mg/25mg)
Marketing Category : DRUG FOR FURTHER PROCESSING
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Details:
TNKase (tenecteplase) is a tissue plasminogen activator, indicated to reduce the risk of death associated with acute ST elevation myocardial infarction (STEMI).
Lead Product(s): Tenecteplase
Therapeutic Area: Neurology Brand Name: TNKase
Study Phase: Approved FDFProduct Type: Enzyme
Sponsor: Inapplicable
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable March 03, 2025
Lead Product(s) : Tenecteplase
Therapeutic Area : Neurology
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
FDA Approves Genentech’s TNKase® in Acute Ischemic Stroke in Adults
Details : TNKase (tenecteplase) is a tissue plasminogen activator, indicated to reduce the risk of death associated with acute ST elevation myocardial infarction (STEMI).
Product Name : TNKase
Product Type : Enzyme
Upfront Cash : Inapplicable
March 03, 2025
RLD :
TE Code :
Brand Name : TNKASE
Dosage Form : VIAL
Dosage Strength : 50MG/VIAL
Approval Date :
Application Number : 103909
RX/OTC/DISCN :
RLD :
TE Code :
Regulatory Info :
Registration Country : Sweden
Brand Name : Metalyse
Dosage Form : PULVER OCH VÄTSKA TILL INJEKTIONSVÄTSKA
Dosage Strength : 8000 ENHETER
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Metalyse
Dosage Form : PULVER OCH VÄTSKA TILL INJEKTIONSVÄTSKA
Dosage Strength : 10 000 ENHETER
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Norway
Brand Name : Metalyse
Dosage Form : Powder for solution for injection
Dosage Strength : 5,000 E
Packaging : Vials 5000E
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
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