Package 60951-700-70

Brand: endocet

Generic: oxycodone and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 60951-700-70
Digits Only 6095170070
Product NDC 60951-700
Description

100 TABLET in 1 BOTTLE (60951-700-70)

Marketing

Marketing Status
Discontinued 2028-05-31
Brand endocet
Generic oxycodone and acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "097fa5e7-7122-439a-8ac9-c85766003509", "openfda": {"unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049216", "1049221", "1049223", "1049225", "1049227", "1049635", "1487288"], "spl_set_id": ["944d3e60-7eee-11de-a413-0002a5d5c51b"], "manufacturer_name": ["Par Health USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (60951-700-70)", "package_ndc": "60951-700-70", "marketing_end_date": "20280531", "marketing_start_date": "20030306"}], "brand_name": "ENDOCET", "product_id": "60951-700_097fa5e7-7122-439a-8ac9-c85766003509", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "60951-700", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Par Health USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ENDOCET", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA040330", "marketing_category": "ANDA", "marketing_end_date": "20280531", "marketing_start_date": "20030306"}