Package 63629-1180-1

Brand: hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 63629-1180-1
Digits Only 6362911801
Product NDC 63629-1180
Description

100 TABLET in 1 BOTTLE (63629-1180-1)

Marketing

Marketing Status
Marketed Since 2022-11-09
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": "ffdf8868-26d5-4dea-9e78-fa8055715c74", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["856992"], "spl_set_id": ["f08ea7a7-211e-4e0b-88c3-8f29a567fdc0"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-1180-1)", "package_ndc": "63629-1180-1", "marketing_start_date": "20221109"}], "brand_name": "hydrocodone bitartrate and acetaminophen", "product_id": "63629-1180_ffdf8868-26d5-4dea-9e78-fa8055715c74", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "63629-1180", "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": "7.5 mg/1"}], "application_number": "ANDA207509", "marketing_category": "ANDA", "marketing_start_date": "20190617", "listing_expiration_date": "20261231"}