Package 68462-304-50

Brand: norethindrone acetate

Generic: norethindrone acetate
NDC Package

Package Facts

Identity

Package NDC 68462-304-50
Digits Only 6846230450
Product NDC 68462-304
Description

50 TABLET in 1 BOTTLE (68462-304-50)

Marketing

Marketing Status
Marketed Since 2010-07-21
Brand norethindrone acetate
Generic norethindrone acetate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "61f08f82-c9ec-45cf-ab8b-18afabde75e2", "openfda": {"upc": ["0368462304501"], "unii": ["9S44LIC7OJ"], "rxcui": ["1000405"], "spl_set_id": ["d0a94321-eb60-4aa6-a429-f0156f9f8e01"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (68462-304-05)", "package_ndc": "68462-304-05", "marketing_start_date": "20100721"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (68462-304-50)", "package_ndc": "68462-304-50", "marketing_start_date": "20100721"}], "brand_name": "Norethindrone Acetate", "product_id": "68462-304_61f08f82-c9ec-45cf-ab8b-18afabde75e2", "dosage_form": "TABLET", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "68462-304", "generic_name": "Norethindrone Acetate", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norethindrone Acetate", "active_ingredients": [{"name": "NORETHINDRONE ACETATE", "strength": "5 mg/1"}], "application_number": "ANDA091090", "marketing_category": "ANDA", "marketing_start_date": "20100721", "listing_expiration_date": "20271231"}