Package 70700-101-85

Brand: norethindrone acetate and ethinyl estradiol

Generic: norethindrone acetate and ethinyl estradiol tablets and ferrous fumarate tablets
NDC Package

Package 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
Marketed Since 2018-08-24
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"}