Package 51285-127-97
Brand: loestrin 21 day
Generic: norethindrone acetate and ethinyl estradiolPackage Facts
Identity
Package NDC
51285-127-97
Digits Only
5128512797
Product NDC
51285-127
Description
5 POUCH in 1 CARTON (51285-127-97) / 1 BLISTER PACK in 1 POUCH / 21 TABLET in 1 BLISTER PACK
Marketing
Marketing Status
Brand
loestrin 21 day
Generic
norethindrone acetate and ethinyl estradiol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "21f0dbf2-f0a8-447a-a975-482b4194b1eb", "openfda": {"nui": ["N0000175825", "N0000000100"], "unii": ["9S44LIC7OJ", "423D2T571U"], "rxcui": ["259176", "1358762", "1358763", "1358770", "1358776", "1358781", "1359022", "1359023", "1359026", "1359028", "1359031"], "spl_set_id": ["f29ebcb5-7e65-4092-bfaa-f5ec026fc255"], "pharm_class_epc": ["Estrogen [EPC]"], "pharm_class_moa": ["Estrogen Receptor Agonists [MoA]"], "manufacturer_name": ["Teva Women's Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 POUCH in 1 CARTON (51285-127-97) / 1 BLISTER PACK in 1 POUCH / 21 TABLET in 1 BLISTER PACK", "package_ndc": "51285-127-97", "marketing_start_date": "20150226"}], "brand_name": "Loestrin 21 Day", "product_id": "51285-127_21f0dbf2-f0a8-447a-a975-482b4194b1eb", "dosage_form": "TABLET", "pharm_class": ["Estrogen Receptor Agonists [MoA]", "Estrogen [EPC]", "Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "51285-127", "generic_name": "Norethindrone Acetate and Ethinyl Estradiol", "labeler_name": "Teva Women's Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Loestrin", "brand_name_suffix": "21 Day", "active_ingredients": [{"name": "ETHINYL ESTRADIOL", "strength": "30 ug/1"}, {"name": "NORETHINDRONE ACETATE", "strength": "1.5 mg/1"}], "application_number": "ANDA076381", "marketing_category": "ANDA", "marketing_start_date": "20150226", "listing_expiration_date": "20261231"}