Package 72189-579-60

Brand: buprenorphine sublingual

Generic: buprenorphine sublingual
NDC Package

Package Facts

Identity

Package NDC 72189-579-60
Digits Only 7218957960
Product NDC 72189-579
Product ID 72189-579_2204e135-6a0d-68a2-e063-6394a90ac019
Description

60 TABLET in 1 BOTTLE (72189-579-60)

Marketing

Marketing Status
Marketed Since 2024-09-13
Brand buprenorphine sublingual
Generic buprenorphine sublingual
Sample Package No

Linked Drug Pages (1)

Buprenorphine Sublingual ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["SUBLINGUAL"], "spl_id": "2204e135-6a0d-68a2-e063-6394a90ac019", "openfda": {"unii": ["56W8MW3EN1"], "rxcui": ["351264"], "spl_set_id": ["2204e135-6a0c-68a2-e063-6394a90ac019"], "manufacturer_name": ["Direct_rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-579-60)", "package_ndc": "72189-579-60", "marketing_start_date": "20240913"}], "brand_name": "Buprenorphine Sublingual", "product_id": "72189-579_2204e135-6a0d-68a2-e063-6394a90ac019", "dosage_form": "TABLET", "pharm_class": ["Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "72189-579", "dea_schedule": "CIII", "generic_name": "Buprenorphine Sublingual", "labeler_name": "Direct_rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buprenorphine Sublingual", "active_ingredients": [{"name": "BUPRENORPHINE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA201760", "marketing_category": "ANDA", "marketing_start_date": "20240913", "listing_expiration_date": "20261231"}