Package 0555-0211-10

Brand: norethindrone acetate

Generic: norethindrone acetate
NDC Package

Package Facts

Identity

Package NDC 0555-0211-10
Digits Only 0555021110
Product NDC 0555-0211
Product ID 0555-0211_953441f0-0a24-40ba-a433-1de55da3ebaa
Description

50 TABLET in 1 BOTTLE (0555-0211-10)

Marketing

Marketing Status
Marketed Since 2001-06-29
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": "953441f0-0a24-40ba-a433-1de55da3ebaa", "openfda": {"unii": ["9S44LIC7OJ"], "rxcui": ["1000405"], "spl_set_id": ["f73f9807-4af6-4faa-ba9a-656a47a4c5e0"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (0555-0211-10)", "package_ndc": "0555-0211-10", "marketing_start_date": "20010629"}], "brand_name": "Norethindrone Acetate", "product_id": "0555-0211_953441f0-0a24-40ba-a433-1de55da3ebaa", "dosage_form": "TABLET", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "0555-0211", "generic_name": "Norethindrone Acetate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norethindrone Acetate", "active_ingredients": [{"name": "NORETHINDRONE ACETATE", "strength": "5 mg/1"}], "application_number": "ANDA075951", "marketing_category": "ANDA", "marketing_start_date": "20010629", "listing_expiration_date": "20261231"}