Package 72162-1289-1

Brand: hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 72162-1289-1
Digits Only 7216212891
Product NDC 72162-1289
Product ID 72162-1289_33d10c89-8753-4a17-8940-0ea30e4d2b75
Description

100 TABLET in 1 BOTTLE, PLASTIC (72162-1289-1)

Marketing

Marketing Status
Marketed Since 2016-04-07
Brand hydrocodone bitartrate and acetaminophen
Generic hydrocodone bitartrate and acetaminophen
Sample Package No

Linked Drug Pages (1)

Hydrocodone Bitartrate and Acetaminophen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "33d10c89-8753-4a17-8940-0ea30e4d2b75", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["856980"], "spl_set_id": ["e5d6de20-c195-4b97-963a-2f3832e50b49"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72162-1289-1)", "package_ndc": "72162-1289-1", "marketing_start_date": "20160407"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "72162-1289_33d10c89-8753-4a17-8940-0ea30e4d2b75", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "72162-1289", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "300 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "10 mg/1"}], "application_number": "ANDA202214", "marketing_category": "ANDA", "marketing_start_date": "20160407", "listing_expiration_date": "20261231"}