Package 50090-1778-0

Brand: hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 50090-1778-0
Digits Only 5009017780
Product NDC 50090-1778
Description

20 TABLET in 1 BOTTLE (50090-1778-0)

Marketing

Marketing Status
Marketed Since 2015-04-14
Brand hydrocodone bitartrate and acetaminophen
Generic hydrocodone bitartrate and acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4eef7fec-90bb-4910-8ace-b3d3656c7273", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857002"], "spl_set_id": ["fc61200e-cc40-47c4-8792-c939c9877ae2"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (50090-1778-0)", "package_ndc": "50090-1778-0", "marketing_start_date": "20150414"}, {"sample": false, "description": "12 TABLET in 1 BOTTLE (50090-1778-7)", "package_ndc": "50090-1778-7", "marketing_start_date": "20190129"}], "brand_name": "HYDROCODONE BITARTRATE AND ACETAMINOPHEN", "product_id": "50090-1778_4eef7fec-90bb-4910-8ace-b3d3656c7273", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "50090-1778", "dea_schedule": "CII", "generic_name": "HYDROCODONE BITARTRATE AND ACETAMINOPHEN", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROCODONE BITARTRATE AND ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "5 mg/1"}], "application_number": "ANDA040409", "marketing_category": "ANDA", "marketing_start_date": "20001020", "listing_expiration_date": "20271231"}