Package 58118-4459-8

Brand: buprenorphine

Generic: buprenorphine
NDC Package

Package Facts

Identity

Package NDC 58118-4459-8
Digits Only 5811844598
Product NDC 58118-4459
Product ID 58118-4459_2e5a8bb5-e89c-7e3e-e063-6294a90a6b18
Description

30 TABLET in 1 BLISTER PACK (58118-4459-8)

Marketing

Marketing Status
Marketed Since 2025-02-17
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": "2e5a8bb5-e89c-7e3e-e063-6294a90a6b18", "openfda": {"unii": ["56W8MW3EN1"], "rxcui": ["351264"], "spl_set_id": ["9d976ee7-9509-49da-89fd-48d7e712697b"], "manufacturer_name": ["Clinical Solutions Wholesale, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (58118-4459-8)", "package_ndc": "58118-4459-8", "marketing_start_date": "20250217"}], "brand_name": "Buprenorphine", "product_id": "58118-4459_2e5a8bb5-e89c-7e3e-e063-6294a90a6b18", "dosage_form": "TABLET", "pharm_class": ["Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "58118-4459", "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": "ANDA201760", "marketing_category": "ANDA", "marketing_start_date": "20160217", "listing_expiration_date": "20261231"}