Package 72887-648-12

Brand: oxycodone hydrochloride and acetaminophen

Generic: oxycodone hydrochloride and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 72887-648-12
Digits Only 7288764812
Product NDC 72887-648
Product ID 72887-648_42f2bb2a-1520-86cb-e063-6394a90a3a00
Description

120 mL in 1 BOTTLE, PLASTIC (72887-648-12)

Marketing

Marketing Status
Marketed Since 2020-03-01
Brand oxycodone hydrochloride and acetaminophen
Generic oxycodone hydrochloride and acetaminophen
Sample Package No

Linked Drug Pages (1)

oxycodone hydrochloride and acetaminophen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "42f2bb2a-1520-86cb-e063-6394a90a3a00", "openfda": {"upc": ["0372887648126"], "unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["2105822"], "spl_set_id": ["96b0067e-aabe-df4f-e053-2995a90a4a86"], "manufacturer_name": ["FH2 Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 mL in 1 BOTTLE, PLASTIC (72887-648-12)", "package_ndc": "72887-648-12", "marketing_start_date": "20200301"}], "brand_name": "oxycodone hydrochloride and acetaminophen", "product_id": "72887-648_42f2bb2a-1520-86cb-e063-6394a90a3a00", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72887-648", "dea_schedule": "CII", "generic_name": "oxycodone hydrochloride and acetaminophen", "labeler_name": "FH2 Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "oxycodone hydrochloride and acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "300 mg/5mL"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA202142", "marketing_category": "ANDA", "marketing_start_date": "20200301", "listing_expiration_date": "20261231"}