Package 70700-101-85
Brand: norethindrone acetate and ethinyl estradiol
Generic: norethindrone acetate and ethinyl estradiol tablets and ferrous fumarate tabletsPackage Facts
Identity
Package NDC
70700-101-85
Digits Only
7070010185
Product NDC
70700-101
Description
3 BLISTER PACK in 1 CARTON (70700-101-85) / 1 KIT in 1 BLISTER PACK
Marketing
Marketing Status
Brand
norethindrone acetate and ethinyl estradiol
Generic
norethindrone acetate and ethinyl estradiol tablets and ferrous fumarate tablets
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0b7a2fac-2281-4c64-29aa-5e0d05d49236", "openfda": {"rxcui": ["259176", "1426288", "1426600"], "spl_set_id": ["b4bc4302-9484-465a-090d-47e1e0360b73"], "manufacturer_name": ["Xiromed, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (70700-101-85) / 1 KIT in 1 BLISTER PACK", "package_ndc": "70700-101-85", "marketing_start_date": "20180824"}], "brand_name": "Norethindrone Acetate and Ethinyl Estradiol", "product_id": "70700-101_0b7a2fac-2281-4c64-29aa-5e0d05d49236", "dosage_form": "KIT", "product_ndc": "70700-101", "generic_name": "Norethindrone Acetate and Ethinyl Estradiol Tablets and Ferrous Fumarate Tablets", "labeler_name": "Xiromed, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norethindrone Acetate and Ethinyl Estradiol", "application_number": "ANDA209609", "marketing_category": "ANDA", "marketing_start_date": "20180824", "listing_expiration_date": "20261231"}