Package 72162-1344-3

Brand: buprenorphine

Generic: buprenorphine
NDC Package

Package Facts

Identity

Package NDC 72162-1344-3
Digits Only 7216213443
Product NDC 72162-1344
Product ID 72162-1344_86e7bced-d51f-4e0b-9a33-4a1ea331f2c4
Description

30 TABLET in 1 BOTTLE (72162-1344-3)

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": "86e7bced-d51f-4e0b-9a33-4a1ea331f2c4", "openfda": {"unii": ["56W8MW3EN1"], "rxcui": ["351264"], "spl_set_id": ["cd0a90c6-32cc-4114-8573-86ac85503bdf"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-1344-3)", "package_ndc": "72162-1344-3", "marketing_start_date": "20240111"}], "brand_name": "BUPRENORPHINE", "product_id": "72162-1344_86e7bced-d51f-4e0b-9a33-4a1ea331f2c4", "dosage_form": "TABLET", "pharm_class": ["Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "72162-1344", "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": "2 mg/1"}], "application_number": "ANDA207276", "marketing_category": "ANDA", "marketing_start_date": "20171025", "listing_expiration_date": "20261231"}