Package 71335-1470-3

Brand: hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 71335-1470-3
Digits Only 7133514703
Product NDC 71335-1470
Description

18 TABLET in 1 BOTTLE (71335-1470-3)

Marketing

Marketing Status
Marketed Since 2024-08-12
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": "07ec0b02-5410-4802-bd12-68e52f2426e5", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857002"], "spl_set_id": ["25d49886-9f9a-4015-bca2-9190b30d9120"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE (71335-1470-1)", "package_ndc": "71335-1470-1", "marketing_start_date": "20200114"}, {"sample": false, "description": "12 TABLET in 1 BOTTLE (71335-1470-2)", "package_ndc": "71335-1470-2", "marketing_start_date": "20200819"}, {"sample": false, "description": "18 TABLET in 1 BOTTLE (71335-1470-3)", "package_ndc": "71335-1470-3", "marketing_start_date": "20240812"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "71335-1470_07ec0b02-5410-4802-bd12-68e52f2426e5", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "71335-1470", "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": "5 mg/1"}], "application_number": "ANDA202991", "marketing_category": "ANDA", "marketing_start_date": "20160412", "listing_expiration_date": "20261231"}