Package 50090-6161-0

Brand: norethindrone

Generic: norethindrone
NDC Package

Package Facts

Identity

Package NDC 50090-6161-0
Digits Only 5009061610
Product NDC 50090-6161
Description

1 BLISTER PACK in 1 CARTON (50090-6161-0) / 28 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2022-10-11
Brand norethindrone
Generic norethindrone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9dc94f9a-0113-49fe-9500-2a96808b9888", "openfda": {"nui": ["M0447349", "N0000175602"], "unii": ["T18F433X4S"], "rxcui": ["198042", "748961"], "spl_set_id": ["70231aa1-9dd2-420f-9cb3-432d3c2477d1"], "pharm_class_cs": ["Progesterone Congeners [CS]"], "pharm_class_epc": ["Progestin [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50090-6161-0)  / 28 TABLET in 1 BLISTER PACK", "package_ndc": "50090-6161-0", "marketing_start_date": "20221011"}], "brand_name": "NORETHINDRONE", "product_id": "50090-6161_9dc94f9a-0113-49fe-9500-2a96808b9888", "dosage_form": "TABLET", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "50090-6161", "generic_name": "NORETHINDRONE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NORETHINDRONE", "active_ingredients": [{"name": "NORETHINDRONE", "strength": ".35 mg/1"}], "application_number": "ANDA091325", "marketing_category": "ANDA", "marketing_start_date": "20201111", "listing_expiration_date": "20261231"}