Package 62756-459-83

Brand: buprenorphine

Generic: buprenorphine
NDC Package

Package Facts

Identity

Package NDC 62756-459-83
Digits Only 6275645983
Product NDC 62756-459
Product ID 62756-459_ba293490-0f6f-4400-82cd-3af9774839e8
Description

30 TABLET in 1 BOTTLE (62756-459-83)

Marketing

Marketing Status
Marketed Since 2016-02-17
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": "ba293490-0f6f-4400-82cd-3af9774839e8", "openfda": {"unii": ["56W8MW3EN1"], "rxcui": ["351264", "351265"], "spl_set_id": ["9fd1f18f-0b0f-4059-b603-19ecbf0ed63a"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (62756-459-64)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "62756-459-64", "marketing_start_date": "20160217"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (62756-459-83)", "package_ndc": "62756-459-83", "marketing_start_date": "20160217"}], "brand_name": "Buprenorphine", "product_id": "62756-459_ba293490-0f6f-4400-82cd-3af9774839e8", "dosage_form": "TABLET", "pharm_class": ["Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "62756-459", "dea_schedule": "CIII", "generic_name": "Buprenorphine", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buprenorphine", "active_ingredients": [{"name": "BUPRENORPHINE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA201760", "marketing_category": "ANDA", "marketing_start_date": "20160217", "listing_expiration_date": "20271231"}