Package 58118-0176-8

Brand: buprenorphine hcl

Generic: buprenorphine hcl
NDC Package

Package Facts

Identity

Package NDC 58118-0176-8
Digits Only 5811801768
Product NDC 58118-0176
Product ID 58118-0176_0e76c642-8fc8-c0b6-e063-6394a90a413e
Description

30 TABLET in 1 BLISTER PACK (58118-0176-8)

Marketing

Marketing Status
Marketed Since 2018-10-15
Brand buprenorphine hcl
Generic buprenorphine hcl
Sample Package No

Linked Drug Pages (1)

Buprenorphine HCl ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["SUBLINGUAL"], "spl_id": "0e76c642-8fc8-c0b6-e063-6394a90a413e", "openfda": {"unii": ["56W8MW3EN1"], "rxcui": ["351264", "351265"], "spl_set_id": ["3a7418a2-bd6e-4082-b0fe-a5498e7b944a"], "manufacturer_name": ["Clinical Solutions Wholesale, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (58118-0176-8)", "package_ndc": "58118-0176-8", "marketing_start_date": "20181015"}], "brand_name": "Buprenorphine HCl", "product_id": "58118-0176_0e76c642-8fc8-c0b6-e063-6394a90a413e", "dosage_form": "TABLET", "pharm_class": ["Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "58118-0176", "dea_schedule": "CIII", "generic_name": "Buprenorphine HCl", "labeler_name": "Clinical Solutions Wholesale, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buprenorphine HCl", "active_ingredients": [{"name": "BUPRENORPHINE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA078633", "marketing_category": "ANDA", "marketing_start_date": "20091008", "listing_expiration_date": "20261231"}