Package 72189-191-30

Brand: hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 72189-191-30
Digits Only 7218919130
Product NDC 72189-191
Product ID 72189-191_2be977e6-4cfd-9a64-e063-6294a90a9fc9
Description

30 TABLET in 1 BOTTLE (72189-191-30)

Marketing

Marketing Status
Marketed Since 2021-09-15
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": "2be977e6-4cfd-9a64-e063-6294a90a9fc9", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857005"], "spl_set_id": ["cc0e654d-1eaa-7d17-e053-2995a90ab1db"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-191-30)", "package_ndc": "72189-191-30", "marketing_start_date": "20210915"}], "brand_name": "HYDROCODONE BITARTRATE AND ACETAMINOPHEN", "product_id": "72189-191_2be977e6-4cfd-9a64-e063-6294a90a9fc9", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "72189-191", "dea_schedule": "CII", "generic_name": "HYDROCODONE BITARTRATE AND ACETAMINOPHEN", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROCODONE BITARTRATE AND ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "7.5 mg/1"}], "application_number": "ANDA209037", "marketing_category": "ANDA", "marketing_start_date": "20210915", "listing_expiration_date": "20261231"}