Package 72162-1345-3

Brand: buprenorphine

Generic: buprenorphine
NDC Package

Package Facts

Identity

Package NDC 72162-1345-3
Digits Only 7216213453
Product NDC 72162-1345
Product ID 72162-1345_db80352d-ec8c-4f72-aab3-35e68dfdd92e
Description

30 TABLET in 1 BOTTLE (72162-1345-3)

Marketing

Marketing Status
Marketed Since 2024-01-11
Brand buprenorphine
Generic buprenorphine
Sample Package No

Linked Drug Pages (1)

BUPRENORPHINE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["SUBLINGUAL"], "spl_id": "db80352d-ec8c-4f72-aab3-35e68dfdd92e", "openfda": {"unii": ["56W8MW3EN1"], "rxcui": ["351265"], "spl_set_id": ["966adb01-71b4-4e0b-bbc6-b83da9987aa2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-1345-3)", "package_ndc": "72162-1345-3", "marketing_start_date": "20240111"}], "brand_name": "BUPRENORPHINE", "product_id": "72162-1345_db80352d-ec8c-4f72-aab3-35e68dfdd92e", "dosage_form": "TABLET", "pharm_class": ["Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "72162-1345", "dea_schedule": "CIII", "generic_name": "BUPRENORPHINE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUPRENORPHINE", "active_ingredients": [{"name": "BUPRENORPHINE HYDROCHLORIDE", "strength": "8 mg/1"}], "application_number": "ANDA207276", "marketing_category": "ANDA", "marketing_start_date": "20171025", "listing_expiration_date": "20261231"}