Package 71335-2238-1

Brand: hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 71335-2238-1
Digits Only 7133522381
Product NDC 71335-2238
Description

21 TABLET in 1 BOTTLE, PLASTIC (71335-2238-1)

Marketing

Marketing Status
Marketed Since 2024-05-28
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": "68676d8d-aa74-4e23-8a1d-7f4934a68db6", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857005"], "spl_set_id": ["375c3f81-3276-431e-8773-7b189730e9fd"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE, PLASTIC (71335-2238-1)", "package_ndc": "71335-2238-1", "marketing_start_date": "20240528"}, {"sample": false, "description": "36 TABLET in 1 BOTTLE, PLASTIC (71335-2238-2)", "package_ndc": "71335-2238-2", "marketing_start_date": "20240528"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "71335-2238_68676d8d-aa74-4e23-8a1d-7f4934a68db6", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "71335-2238", "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"}