Package 68462-132-81

{"route": ["ORAL"], "spl_id": "0f4e690d-1b9a-4c51-ac0a-8aa783056a00", "openfda": {"nui": ["N0000175825", "N0000000100"], "upc": ["0368462132814", "0368462132791"], "unii": ["423D2T571U", "9S44LIC7OJ"], "rxcui": ["1358762", "1358776"], "spl_set_id": ["5a44f7a2-45f1-4d28-b9fb-61d9f2456422"], "pharm_class_epc": ["Estrogen [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 (68462-132-81)  / 1 BLISTER PACK in 1 POUCH (68462-132-79)  / 21 TABLET in 1 BLISTER PACK", "package_ndc": "68462-132-81", "marketing_start_date": "20160120"}], "brand_name": "Norethindrone Acetate and Ethinyl Estradiol", "product_id": "68462-132_0f4e690d-1b9a-4c51-ac0a-8aa783056a00", "dosage_form": "TABLET", "pharm_class": ["Estrogen Receptor Agonists [MoA]", "Estrogen [EPC]", "Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "68462-132", "generic_name": "Norethindrone Acetate and Ethinyl Estradiol", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norethindrone Acetate and Ethinyl Estradiol", "active_ingredients": [{"name": "ETHINYL ESTRADIOL", "strength": ".02 mg/1"}, {"name": "NORETHINDRONE ACETATE", "strength": "1 mg/1"}], "application_number": "ANDA206969", "marketing_category": "ANDA", "marketing_start_date": "20160120", "listing_expiration_date": "20271231"}