Package 68462-637-29

Brand: levonorgestrel and ethinyl estradiol

Generic: levonorgestrel and ethinyl estradiol
NDC Package

Package Facts

Identity

Package NDC 68462-637-29
Digits Only 6846263729
Product NDC 68462-637
Description

3 POUCH in 1 CARTON (68462-637-29) / 1 BLISTER PACK in 1 POUCH (68462-637-84) / 28 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2015-04-09
Brand levonorgestrel and ethinyl estradiol
Generic levonorgestrel and ethinyl estradiol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ed921f2c-7961-477a-bbac-2e666d32e3ba", "openfda": {"nui": ["N0000175825", "N0000000100", "N0000175830", "M0447349", "N0000175602", "N0000175832"], "upc": ["0368462637296", "0368462637845"], "unii": ["423D2T571U", "5W7SIA7YZW"], "rxcui": ["722152", "751553"], "spl_set_id": ["44fbc5ae-5682-471f-a12a-955e8b4d233a"], "pharm_class_cs": ["Progesterone Congeners [CS]"], "pharm_class_pe": ["Inhibit Ovum Fertilization [PE]"], "pharm_class_epc": ["Estrogen [EPC]", "Progestin [EPC]", "Progestin-containing Intrauterine System [EPC]"], "pharm_class_moa": ["Estrogen Receptor Agonists [MoA]"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 POUCH in 1 CARTON (68462-637-29)  / 1 BLISTER PACK in 1 POUCH (68462-637-84)  / 28 TABLET in 1 BLISTER PACK", "package_ndc": "68462-637-29", "marketing_start_date": "20150409"}], "brand_name": "Levonorgestrel and Ethinyl Estradiol", "product_id": "68462-637_ed921f2c-7961-477a-bbac-2e666d32e3ba", "dosage_form": "TABLET", "pharm_class": ["Estrogen Receptor Agonists [MoA]", "Estrogen [EPC]", "Inhibit Ovum Fertilization [PE]", "Progesterone Congeners [CS]", "Progesterone Congeners [CS]", "Progestin [EPC]", "Progestin-containing Intrauterine System [EPC]"], "product_ndc": "68462-637", "generic_name": "Levonorgestrel and Ethinyl Estradiol", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levonorgestrel and Ethinyl Estradiol", "active_ingredients": [{"name": "ETHINYL ESTRADIOL", "strength": "20 ug/1"}, {"name": "LEVONORGESTREL", "strength": "90 ug/1"}], "application_number": "ANDA202791", "marketing_category": "ANDA", "marketing_start_date": "20150409", "listing_expiration_date": "20271231"}