Package 12496-1208-3

Brand: suboxone

Generic: buprenorphine hydrochloride, naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 12496-1208-3
Digits Only 1249612083
Product NDC 12496-1208
Product ID 12496-1208_ad5a289a-6285-4b2d-b7ad-e4812169dd58
Description

30 POUCH in 1 CARTON (12496-1208-3) / 1 FILM, SOLUBLE in 1 POUCH (12496-1208-1)

Marketing

Marketing Status
Marketed Since 2010-09-13
Brand suboxone
Generic buprenorphine hydrochloride, naloxone hydrochloride
Sample Package No

Linked Drug Pages (1)

Suboxone ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["BUCCAL", "SUBLINGUAL"], "spl_id": "ad5a289a-6285-4b2d-b7ad-e4812169dd58", "openfda": {"upc": ["0312496120835"], "unii": ["56W8MW3EN1", "F850569PQR"], "rxcui": ["1010600", "1010603", "1010604", "1010606", "1307056", "1307058", "1307061", "1307063"], "spl_set_id": ["8a5edcf9-828c-4f97-b671-268ab13a8ecd"], "manufacturer_name": ["INDIVIOR INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (12496-1208-3)  / 1 FILM, SOLUBLE in 1 POUCH (12496-1208-1)", "package_ndc": "12496-1208-3", "marketing_start_date": "20100913"}], "brand_name": "Suboxone", "product_id": "12496-1208_ad5a289a-6285-4b2d-b7ad-e4812169dd58", "dosage_form": "FILM, SOLUBLE", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]", "Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "12496-1208", "dea_schedule": "CIII", "generic_name": "buprenorphine hydrochloride, naloxone hydrochloride", "labeler_name": "INDIVIOR INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Suboxone", "active_ingredients": [{"name": "BUPRENORPHINE HYDROCHLORIDE", "strength": "8 mg/1"}, {"name": "NALOXONE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "NDA022410", "marketing_category": "NDA", "marketing_start_date": "20100913", "listing_expiration_date": "20271231"}