Package 70518-1566-0

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1566-0
Digits Only 7051815660
Product NDC 70518-1566
Product ID 70518-1566_4a644415-533a-ac6e-e063-6294a90aff70
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1566-0)

Marketing

Marketing Status
Marketed Since 2018-12-22
Brand bupropion hydrochloride
Generic bupropion hydrochloride
Sample Package No

Linked Drug Pages (1)

Bupropion Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4a644415-533a-ac6e-e063-6294a90aff70", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993691"], "spl_set_id": ["3b73d56e-e558-49de-8126-d7ec9b67a086"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1566-0)", "package_ndc": "70518-1566-0", "marketing_start_date": "20181222"}], "brand_name": "Bupropion Hydrochloride", "product_id": "70518-1566_4a644415-533a-ac6e-e063-6294a90aff70", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "70518-1566", "generic_name": "Bupropion Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA076143", "marketing_category": "ANDA", "marketing_start_date": "20181222", "listing_expiration_date": "20271231"}