Package 67296-2093-1

Brand: hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 67296-2093-1
Digits Only 6729620931
Product NDC 67296-2093
Description

118 mL in 1 BOTTLE (67296-2093-1)

Marketing

Marketing Status
Marketed Since 2023-10-15
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": "325288e1-687b-6b31-e063-6394a90a8da9", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["856940"], "spl_set_id": ["1535f903-8bd0-c09e-e063-6294a90a4d4d"], "manufacturer_name": ["Redpharm drug"]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE (67296-2093-1)", "package_ndc": "67296-2093-1", "marketing_start_date": "20231015"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "67296-2093_325288e1-687b-6b31-e063-6394a90a8da9", "dosage_form": "SOLUTION", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "67296-2093", "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": "ANDA040838", "marketing_category": "ANDA", "marketing_start_date": "20231015", "listing_expiration_date": "20261231"}