Package 0555-9032-70

Brand: tri-legest fe 28 day

Generic: norethindrone acetate and ethinyl estradiol
NDC Package

Package Facts

Identity

Package NDC 0555-9032-70
Digits Only 0555903270
Product NDC 0555-9032
Description

5 BLISTER PACK in 1 CARTON (0555-9032-70) / 1 KIT in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2007-10-26
Brand tri-legest fe 28 day
Generic norethindrone acetate and ethinyl estradiol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "d7c6f988-bb93-48d0-90e3-9074a5185999", "openfda": {"rxcui": ["259176", "1358762", "1359130", "1359131", "1359132", "1359135"], "spl_set_id": ["6f9d30d9-5553-4cbd-a099-ff045bc85821"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 BLISTER PACK in 1 CARTON (0555-9032-70)  / 1 KIT in 1 BLISTER PACK", "package_ndc": "0555-9032-70", "marketing_start_date": "20071026"}], "brand_name": "Tri-Legest Fe 28 Day", "product_id": "0555-9032_d7c6f988-bb93-48d0-90e3-9074a5185999", "dosage_form": "KIT", "product_ndc": "0555-9032", "generic_name": "Norethindrone Acetate and Ethinyl Estradiol", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tri-Legest Fe", "brand_name_suffix": "28 Day", "application_number": "ANDA076105", "marketing_category": "ANDA", "marketing_start_date": "20071026", "listing_expiration_date": "20261231"}