Package 0143-9246-05

Brand: buprenorphine hydrochloride

Generic: buprenorphine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0143-9246-05
Digits Only 0143924605
Product NDC 0143-9246
Product ID 0143-9246_8ba9787c-d429-4a5d-8424-e13be15cb9f1
Description

5 VIAL in 1 CARTON (0143-9246-05) / 1 mL in 1 VIAL (0143-9246-01)

Marketing

Marketing Status
Marketed Since 2019-07-12
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": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "8ba9787c-d429-4a5d-8424-e13be15cb9f1", "openfda": {"unii": ["56W8MW3EN1"], "rxcui": ["238129"], "spl_set_id": ["adc1167e-910e-4d7b-abdc-751d3df0c3dc"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL in 1 CARTON (0143-9246-05)  / 1 mL in 1 VIAL (0143-9246-01)", "package_ndc": "0143-9246-05", "marketing_start_date": "20190712"}], "brand_name": "Buprenorphine Hydrochloride", "product_id": "0143-9246_8ba9787c-d429-4a5d-8424-e13be15cb9f1", "dosage_form": "INJECTION", "pharm_class": ["Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "0143-9246", "dea_schedule": "CIII", "generic_name": "Buprenorphine Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buprenorphine Hydrochloride", "active_ingredients": [{"name": "BUPRENORPHINE HYDROCHLORIDE", "strength": ".324 mg/mL"}], "application_number": "ANDA076931", "marketing_category": "ANDA", "marketing_start_date": "20050525", "listing_expiration_date": "20261231"}