Package 50090-7559-0

Brand: buprenorphine hydrochloride

Generic: buprenorphine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7559-0
Digits Only 5009075590
Product NDC 50090-7559
Product ID 50090-7559_18fa8a54-6196-4635-a213-f78a9236f3d6
Description

30 TABLET in 1 BOTTLE (50090-7559-0)

Marketing

Marketing Status
Marketed Since 2025-05-27
Brand buprenorphine hydrochloride
Generic buprenorphine hydrochloride
Sample Package No

Linked Drug Pages (1)

buprenorphine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["SUBLINGUAL"], "spl_id": "18fa8a54-6196-4635-a213-f78a9236f3d6", "openfda": {"unii": ["56W8MW3EN1"], "rxcui": ["351265"], "spl_set_id": ["c1398d85-d4bb-4426-8ecf-a50400910d81"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7559-0)", "package_ndc": "50090-7559-0", "marketing_start_date": "20250527"}], "brand_name": "buprenorphine hydrochloride", "product_id": "50090-7559_18fa8a54-6196-4635-a213-f78a9236f3d6", "dosage_form": "TABLET", "pharm_class": ["Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "50090-7559", "dea_schedule": "CIII", "generic_name": "buprenorphine hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "buprenorphine hydrochloride", "active_ingredients": [{"name": "BUPRENORPHINE HYDROCHLORIDE", "strength": "8 mg/1"}], "application_number": "ANDA090622", "marketing_category": "ANDA", "marketing_start_date": "20231012", "listing_expiration_date": "20261231"}