Package 65162-033-50

Brand: acetaminophen and codeine

Generic: acetaminophen and codeine
NDC Package

Package Facts

Identity

Package NDC 65162-033-50
Digits Only 6516203350
Product NDC 65162-033
Description

500 TABLET in 1 BOTTLE (65162-033-50)

Marketing

Marketing Status
Marketed Since 2008-05-29
Brand acetaminophen and codeine
Generic acetaminophen and codeine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "75a6d334-42b8-44d0-a4a1-fd3eeb95008f", "openfda": {"upc": ["0365162033106"], "unii": ["362O9ITL9D", "GSL05Y1MN6"], "rxcui": ["993781"], "spl_set_id": ["8bc4108b-314e-4a52-a37c-631c6b869b04"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65162-033-10)", "package_ndc": "65162-033-10", "marketing_start_date": "20080529"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65162-033-11)", "package_ndc": "65162-033-11", "marketing_start_date": "20080529"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (65162-033-50)", "package_ndc": "65162-033-50", "marketing_start_date": "20080529"}], "brand_name": "Acetaminophen and Codeine", "product_id": "65162-033_75a6d334-42b8-44d0-a4a1-fd3eeb95008f", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "65162-033", "dea_schedule": "CIII", "generic_name": "Acetaminophen and Codeine", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetaminophen and Codeine", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "300 mg/1"}, {"name": "CODEINE PHOSPHATE", "strength": "30 mg/1"}], "application_number": "ANDA040779", "marketing_category": "ANDA", "marketing_start_date": "20080529", "listing_expiration_date": "20261231"}