NDC 50242-120

TNKase

Tenecteplase

TNKase is a Kit in the Human Prescription Drug category. It is labeled and distributed by Genentech, Inc.. The primary component is .

• Product ID: 50242-120_08edc27c-7dbb-4493-b12d-aa2f97124839
• NDC: 50242-120
• Product Type: Human Prescription Drug
• Proprietary Name: TNKase
• Generic Name: Tenecteplase
• Dosage Form: Kit
• Marketing Start Date: 2018-11-07
• Marketing Category: BLA / BLA
• Application Number: BLA103909
• Labeler Name: Genentech, Inc.
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 50242-120-47

1 KIT in 1 CARTON (50242-120-47) * 1 VIAL, SINGLE-USE in 1 CARTON (50242-037-06) > 50 mg in 1 VIAL, SINGLE-USE * 1 VIAL, SINGLE-USE in 1 CARTON (50242-901-09) > 10 mL in 1 VIAL, SINGLE-USE

• Marketing Start Date: 2018-11-07
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 50242-120-01 [50242012001]

TNKase KIT

• Marketing Category: BLA
• Application Number: BLA103909
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2000-06-02

NDC 50242-120-47 [50242012047]

TNKase KIT

• Marketing Category: BLA
• Application Number: BLA103909
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-11-07

Drug Details

OpenFDA Data

• SPL SET ID: 66a1e273-ab59-4e7a-a223-a96b86501f51
• Manufacturer:
  • Genentech, Inc.
• RxNorm Concept Unique ID - RxCUI:
  • 313212
  • 797544
  • 284422