Package 0069-1975-40

Brand: vyndaqel

Generic: tafamidis meglumine
NDC Package

Package Facts

Identity

Package NDC 0069-1975-40
Digits Only 0069197540
Product NDC 0069-1975
Description

4 CARTON in 1 CARTON (0069-1975-40) / 30 BLISTER PACK in 1 CARTON / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0069-1975-12)

Marketing

Marketing Status
Discontinued 2027-07-31
Brand vyndaqel
Generic tafamidis meglumine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ee63a96-9d81-4941-a641-510beb6abb81", "openfda": {"unii": ["ZU7CF08A1A", "8FG9H9D31J"], "rxcui": ["2168534", "2168540", "2168542", "2168548"], "spl_set_id": ["1b4121ee-a733-4456-a917-be2603477839"], "manufacturer_name": ["Pfizer Laboratories Div Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 CARTON in 1 CARTON (0069-1975-40)  / 30 BLISTER PACK in 1 CARTON / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0069-1975-12)", "package_ndc": "0069-1975-40", "marketing_end_date": "20270731", "marketing_start_date": "20190516"}], "brand_name": "Vyndaqel", "product_id": "0069-1975_4ee63a96-9d81-4941-a641-510beb6abb81", "dosage_form": "CAPSULE, LIQUID FILLED", "product_ndc": "0069-1975", "generic_name": "tafamidis meglumine", "labeler_name": "Pfizer Laboratories Div Pfizer Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vyndaqel", "active_ingredients": [{"name": "TAFAMIDIS MEGLUMINE", "strength": "20 mg/1"}], "application_number": "NDA211996", "marketing_category": "NDA", "marketing_end_date": "20270731", "marketing_start_date": "20190516"}