Package 72603-239-01

Brand: dabigatran etexilate

Generic: dabigatran etexilate
NDC Package

Package Facts

Identity

Package NDC 72603-239-01
Digits Only 7260323901
Product NDC 72603-239
Product ID 72603-239_450cc975-a89f-2a41-e063-6394a90aefcf
Description

60 CAPSULE in 1 BOTTLE (72603-239-01)

Marketing

Marketing Status
Marketed Since 2025-12-01
Brand dabigatran etexilate
Generic dabigatran etexilate
Sample Package No

Linked Drug Pages (1)

Dabigatran Etexilate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "450cc975-a89f-2a41-e063-6394a90aefcf", "openfda": {"upc": ["0372603239010"], "unii": ["SC7NUW5IIT"], "rxcui": ["1037045"], "spl_set_id": ["d5937f27-88c7-4c4a-801e-4c8945008982"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (72603-239-01)", "package_ndc": "72603-239-01", "marketing_start_date": "20251201"}], "brand_name": "Dabigatran Etexilate", "product_id": "72603-239_450cc975-a89f-2a41-e063-6394a90aefcf", "dosage_form": "CAPSULE", "pharm_class": ["Direct Thrombin Inhibitor [EPC]", "Thrombin Inhibitors [MoA]"], "product_ndc": "72603-239", "generic_name": "Dabigatran Etexilate", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dabigatran Etexilate", "active_ingredients": [{"name": "DABIGATRAN ETEXILATE MESYLATE", "strength": "150 mg/1"}], "application_number": "ANDA207961", "marketing_category": "ANDA", "marketing_start_date": "20251201", "listing_expiration_date": "20261231"}