Package 63629-2296-1

Brand: hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 63629-2296-1
Digits Only 6362922961
Product NDC 63629-2296
Product ID 63629-2296_fb02372e-e55a-4ede-b679-6b16538dda95
Description

500 TABLET in 1 BOTTLE, PLASTIC (63629-2296-1)

Marketing

Marketing Status
Marketed Since 2014-10-06
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": "fb02372e-e55a-4ede-b679-6b16538dda95", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857005"], "spl_set_id": ["58f5603e-01c9-44f8-b947-3918fd14e049"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (63629-2296-1)", "package_ndc": "63629-2296-1", "marketing_start_date": "20141006"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "63629-2296_fb02372e-e55a-4ede-b679-6b16538dda95", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "63629-2296", "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": "325 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "7.5 mg/1"}], "application_number": "ANDA202214", "marketing_category": "ANDA", "marketing_start_date": "20141006", "listing_expiration_date": "20261231"}