Package 42291-650-90

Brand: norethindrone acetate

Generic: norethindrone
NDC Package

Package Facts

Identity

Package NDC 42291-650-90
Digits Only 4229165090
Product NDC 42291-650
Product ID 42291-650_3f07bf1f-a9bc-c5ad-e063-6394a90a7545
Description

90 TABLET in 1 BOTTLE (42291-650-90)

Marketing

Marketing Status
Marketed Since 2013-06-18
Brand norethindrone acetate
Generic norethindrone
Sample Package No

Linked Drug Pages (1)

Norethindrone Acetate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3f07bf1f-a9bc-c5ad-e063-6394a90a7545", "openfda": {"unii": ["9S44LIC7OJ"], "rxcui": ["1000405"], "spl_set_id": ["827c7ef1-a8b7-d0c4-b062-c5154b331a35"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (42291-650-90)", "package_ndc": "42291-650-90", "marketing_start_date": "20130618"}], "brand_name": "Norethindrone Acetate", "product_id": "42291-650_3f07bf1f-a9bc-c5ad-e063-6394a90a7545", "dosage_form": "TABLET", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "42291-650", "generic_name": "Norethindrone", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norethindrone Acetate", "active_ingredients": [{"name": "NORETHINDRONE ACETATE", "strength": "5 mg/1"}], "application_number": "ANDA200275", "marketing_category": "ANDA", "marketing_start_date": "20130618", "listing_expiration_date": "20261231"}