Package 71335-2112-1

Brand: hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 71335-2112-1
Digits Only 7133521121
Product NDC 71335-2112
Description

21 TABLET in 1 BOTTLE (71335-2112-1)

Marketing

Marketing Status
Marketed Since 2022-06-20
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": "c1879bd1-230a-4017-a114-4caaaea0058a", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857005"], "spl_set_id": ["177c4cd8-80dd-4ed7-9e12-dcec70e0278e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE (71335-2112-1)", "package_ndc": "71335-2112-1", "marketing_start_date": "20220620"}, {"sample": false, "description": "36 TABLET in 1 BOTTLE (71335-2112-2)", "package_ndc": "71335-2112-2", "marketing_start_date": "20220620"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-2112-3)", "package_ndc": "71335-2112-3", "marketing_start_date": "20220620"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "71335-2112_c1879bd1-230a-4017-a114-4caaaea0058a", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "71335-2112", "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": "ANDA211487", "marketing_category": "ANDA", "marketing_start_date": "20181108", "listing_expiration_date": "20261231"}