Package 58118-0501-8

Brand: buprenorphine

Generic: buprenorphine
NDC Package

Package Facts

Identity

Package NDC 58118-0501-8
Digits Only 5811805018
Product NDC 58118-0501
Product ID 58118-0501_0e85a5c9-76a8-f621-e063-6394a90a8782
Description

30 TABLET in 1 BLISTER PACK (58118-0501-8)

Marketing

Marketing Status
Marketed Since 2017-10-25
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": "0e85a5c9-76a8-f621-e063-6394a90a8782", "openfda": {"upc": ["0358118050180"], "unii": ["56W8MW3EN1"], "rxcui": ["351264"], "spl_set_id": ["325532f0-276f-4689-97d6-cda879b4c758"], "manufacturer_name": ["Clinical Solutions Wholesale, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (58118-0501-8)", "package_ndc": "58118-0501-8", "marketing_start_date": "20171025"}], "brand_name": "BUPRENORPHINE", "product_id": "58118-0501_0e85a5c9-76a8-f621-e063-6394a90a8782", "dosage_form": "TABLET", "pharm_class": ["Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "58118-0501", "dea_schedule": "CIII", "generic_name": "BUPRENORPHINE", "labeler_name": "Clinical Solutions Wholesale, LLC", "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"}