Package 0069-8730-30

Brand: vyndamax

Generic: tafamidis
NDC Package

Package Facts

Identity

Package NDC 0069-8730-30
Digits Only 0069873030
Product NDC 0069-8730
Product ID 0069-8730_4ee63a96-9d81-4941-a641-510beb6abb81
Description

30 BLISTER PACK in 1 CARTON (0069-8730-30) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0069-8730-01)

Marketing

Marketing Status
Marketed Since 2019-08-27
Brand vyndamax
Generic tafamidis
Sample Package No

Linked Drug Pages (1)

Vyndaqel, Vyndamax ndc-match (0.95)

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": "30 BLISTER PACK in 1 CARTON (0069-8730-30)  / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0069-8730-01)", "package_ndc": "0069-8730-30", "marketing_start_date": "20190827"}], "brand_name": "Vyndamax", "product_id": "0069-8730_4ee63a96-9d81-4941-a641-510beb6abb81", "dosage_form": "CAPSULE, LIQUID FILLED", "product_ndc": "0069-8730", "generic_name": "tafamidis", "labeler_name": "Pfizer Laboratories Div Pfizer Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vyndamax", "active_ingredients": [{"name": "TAFAMIDIS", "strength": "61 mg/1"}], "application_number": "NDA212161", "marketing_category": "NDA", "marketing_start_date": "20190827", "listing_expiration_date": "20271231"}