Package 63629-9475-1

Brand: buprenorphine

Generic: buprenorphine
NDC Package

Package Facts

Identity

Package NDC 63629-9475-1
Digits Only 6362994751
Product NDC 63629-9475
Product ID 63629-9475_0528c316-c40e-4d8e-bb5e-2663faf8a307
Description

30 TABLET in 1 BOTTLE (63629-9475-1)

Marketing

Marketing Status
Marketed Since 2022-11-28
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": "0528c316-c40e-4d8e-bb5e-2663faf8a307", "openfda": {"unii": ["56W8MW3EN1"], "rxcui": ["351264"], "spl_set_id": ["bc5a7137-9e8f-438e-84d9-bdbf1db12998"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-9475-1)", "package_ndc": "63629-9475-1", "marketing_start_date": "20221128"}], "brand_name": "BUPRENORPHINE", "product_id": "63629-9475_0528c316-c40e-4d8e-bb5e-2663faf8a307", "dosage_form": "TABLET", "pharm_class": ["Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "63629-9475", "dea_schedule": "CIII", "generic_name": "BUPRENORPHINE", "labeler_name": "Bryant Ranch Prepack", "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"}