Package 0904-7154-04

Brand: buprenorphine

Generic: buprenorphine
NDC Package

Package Facts

Identity

Package NDC 0904-7154-04
Digits Only 0904715404
Product NDC 0904-7154
Product ID 0904-7154_d28a45db-8ce9-4eef-91ad-2ed508956e59
Description

30 BLISTER PACK in 1 CARTON (0904-7154-04) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2009-10-08
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": "d28a45db-8ce9-4eef-91ad-2ed508956e59", "openfda": {"unii": ["56W8MW3EN1"], "spl_set_id": ["dba586f9-e3f2-4b9c-849b-907c81a5a0ef"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-7154-04)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7154-04", "marketing_start_date": "20091008"}], "brand_name": "Buprenorphine", "product_id": "0904-7154_d28a45db-8ce9-4eef-91ad-2ed508956e59", "dosage_form": "TABLET", "pharm_class": ["Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "0904-7154", "dea_schedule": "CIII", "generic_name": "Buprenorphine", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buprenorphine", "active_ingredients": [{"name": "BUPRENORPHINE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA078633", "marketing_category": "ANDA", "marketing_start_date": "20091008", "listing_expiration_date": "20271231"}