Package 50090-5805-0

Brand: buprenorphine

Generic: buprenorphine
NDC Package

Package Facts

Identity

Package NDC 50090-5805-0
Digits Only 5009058050
Product NDC 50090-5805
Product ID 50090-5805_94b57515-d361-4f99-a7e4-fc5f609426c3
Description

30 TABLET in 1 BOTTLE (50090-5805-0)

Marketing

Marketing Status
Marketed Since 2021-10-15
Brand buprenorphine
Generic buprenorphine
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["SUBLINGUAL"], "spl_id": "94b57515-d361-4f99-a7e4-fc5f609426c3", "openfda": {"unii": ["56W8MW3EN1"], "rxcui": ["351265"], "spl_set_id": ["bfb02ea5-22f2-432e-afc8-f1dbe2ea0614"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-5805-0)", "package_ndc": "50090-5805-0", "marketing_start_date": "20211015"}], "brand_name": "BUPRENORPHINE", "product_id": "50090-5805_94b57515-d361-4f99-a7e4-fc5f609426c3", "dosage_form": "TABLET", "pharm_class": ["Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "50090-5805", "dea_schedule": "CIII", "generic_name": "BUPRENORPHINE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUPRENORPHINE", "active_ingredients": [{"name": "BUPRENORPHINE HYDROCHLORIDE", "strength": "8 mg/1"}], "application_number": "ANDA207276", "marketing_category": "ANDA", "marketing_start_date": "20171025", "listing_expiration_date": "20271231"}