Package 67296-2166-1

Brand: hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 67296-2166-1
Digits Only 6729621661
Product NDC 67296-2166
Description

118 mL in 1 BOTTLE (67296-2166-1)

Marketing

Marketing Status
Marketed Since 2019-04-08
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": "45abe132-b49c-8490-e063-6294a90ad6bf", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["856940"], "spl_set_id": ["37451478-b961-873b-e063-6394a90a7b4e"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE (67296-2166-1)", "package_ndc": "67296-2166-1", "marketing_start_date": "20190408"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "67296-2166_45abe132-b49c-8490-e063-6294a90ad6bf", "dosage_form": "SOLUTION", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "67296-2166", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/15mL"}, {"name": "HYDROCODONE BITARTRATE", "strength": "7.5 mg/15mL"}], "application_number": "ANDA211023", "marketing_category": "ANDA", "marketing_start_date": "20190408", "listing_expiration_date": "20261231"}