Package 72245-193-03

Brand: nalocet

Generic: oxycodone and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 72245-193-03
Digits Only 7224519303
Product NDC 72245-193
Description

30 TABLET in 1 BOTTLE, PLASTIC (72245-193-03)

Marketing

Marketing Status
Marketed Since 2018-05-23
Brand nalocet
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": "1f08bded-8a63-5cb4-e063-6294a90a0a7a", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1037259", "2045500"], "spl_set_id": ["f5f7dfca-a5c7-4445-8a5e-9ec62f33f5be"], "manufacturer_name": ["Forte Bio-Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72245-193-03)", "package_ndc": "72245-193-03", "marketing_start_date": "20180523"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72245-193-10)", "package_ndc": "72245-193-10", "marketing_start_date": "20180523"}], "brand_name": "Nalocet", "product_id": "72245-193_1f08bded-8a63-5cb4-e063-6294a90a0a7a", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72245-193", "dea_schedule": "CII", "generic_name": "oxycodone and acetaminophen", "labeler_name": "Forte Bio-Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nalocet", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "300 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA040608", "marketing_category": "ANDA", "marketing_start_date": "20180523", "listing_expiration_date": "20261231"}