Package 50742-267-50

Brand: norethindrone acetate

Generic: norethindrone acetate
NDC Package

Package Facts

Identity

Package NDC 50742-267-50
Digits Only 5074226750
Product NDC 50742-267
Product ID 50742-267_ec08066e-8299-493e-b502-e56db778b15e
Description

50 TABLET in 1 BOTTLE (50742-267-50)

Marketing

Marketing Status
Marketed Since 2019-08-29
Brand norethindrone acetate
Generic norethindrone acetate
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": "ec08066e-8299-493e-b502-e56db778b15e", "openfda": {"upc": ["0350742267507"], "unii": ["9S44LIC7OJ"], "rxcui": ["1000405"], "spl_set_id": ["2f39b608-cc62-4ff0-a52a-bc3343275269"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (50742-267-50)", "package_ndc": "50742-267-50", "marketing_start_date": "20190829"}], "brand_name": "Norethindrone acetate", "product_id": "50742-267_ec08066e-8299-493e-b502-e56db778b15e", "dosage_form": "TABLET", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "50742-267", "generic_name": "norethindrone acetate", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norethindrone acetate", "active_ingredients": [{"name": "NORETHINDRONE ACETATE", "strength": "5 mg/1"}], "application_number": "ANDA206490", "marketing_category": "ANDA", "marketing_start_date": "20190829", "listing_expiration_date": "20261231"}