Package 70518-2014-0

Brand: buprenorphine hcl

Generic: buprenorphine hcl
NDC Package

Package Facts

Identity

Package NDC 70518-2014-0
Digits Only 7051820140
Product NDC 70518-2014
Product ID 70518-2014_498bf1a2-fabc-0a31-e063-6294a90a6e94
Description

30 TABLET in 1 BLISTER PACK (70518-2014-0)

Marketing

Marketing Status
Marketed Since 2019-04-12
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": "498bf1a2-fabc-0a31-e063-6294a90a6e94", "openfda": {"unii": ["56W8MW3EN1"], "rxcui": ["351265"], "spl_set_id": ["69a647c0-bc09-4ee2-aeb3-ef286caf25e5"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2014-0)", "package_ndc": "70518-2014-0", "marketing_start_date": "20190412"}], "brand_name": "Buprenorphine HCl", "product_id": "70518-2014_498bf1a2-fabc-0a31-e063-6294a90a6e94", "dosage_form": "TABLET", "pharm_class": ["Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "70518-2014", "dea_schedule": "CIII", "generic_name": "Buprenorphine HCl", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buprenorphine HCl", "active_ingredients": [{"name": "BUPRENORPHINE HYDROCHLORIDE", "strength": "8 mg/1"}], "application_number": "ANDA078633", "marketing_category": "ANDA", "marketing_start_date": "20190412", "listing_expiration_date": "20271231"}