Package 63629-9483-1

Brand: buprenorphine and naloxone

Generic: buprenorphine and naloxone
NDC Package

Package Facts

Identity

Package NDC 63629-9483-1
Digits Only 6362994831
Product NDC 63629-9483
Description

30 TABLET in 1 BOTTLE, PLASTIC (63629-9483-1)

Marketing

Marketing Status
Marketed Since 2022-12-12
Brand buprenorphine and naloxone
Generic buprenorphine and naloxone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["SUBLINGUAL"], "spl_id": "6529cd98-61bf-430c-8001-c591d52dfa23", "openfda": {"unii": ["56W8MW3EN1", "5Q187997EE"], "rxcui": ["351267"], "spl_set_id": ["dd3bfccd-86a1-413f-affd-187f81dd07aa"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (63629-9483-1)", "package_ndc": "63629-9483-1", "marketing_start_date": "20221212"}], "brand_name": "Buprenorphine and Naloxone", "product_id": "63629-9483_6529cd98-61bf-430c-8001-c591d52dfa23", "dosage_form": "TABLET", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]", "Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "63629-9483", "dea_schedule": "CIII", "generic_name": "Buprenorphine and Naloxone", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buprenorphine and Naloxone", "active_ingredients": [{"name": "BUPRENORPHINE HYDROCHLORIDE", "strength": "8 mg/1"}, {"name": "NALOXONE HYDROCHLORIDE DIHYDRATE", "strength": "2 mg/1"}], "application_number": "ANDA205601", "marketing_category": "ANDA", "marketing_start_date": "20200413", "listing_expiration_date": "20261231"}