Package 42806-413-60

Brand: bupropion hydrochloride sr

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42806-413-60
Digits Only 4280641360
Product NDC 42806-413
Product ID 42806-413_4bde68a6-0945-b21f-e063-6394a90a3bc4
Description

60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-413-60)

Marketing

Marketing Status
Marketed Since 2023-02-28
Brand bupropion hydrochloride sr
Generic bupropion hydrochloride
Sample Package No

Linked Drug Pages (1)

Bupropion Hydrochloride SR ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4bde68a6-0945-b21f-e063-6394a90a3bc4", "openfda": {"upc": ["0342806413609"], "unii": ["ZG7E5POY8O"], "rxcui": ["1801289"], "spl_set_id": ["f56ccdb1-f9d9-3e5f-e053-2995a90a8f16"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-413-60)", "package_ndc": "42806-413-60", "marketing_start_date": "20230228"}], "brand_name": "Bupropion Hydrochloride SR", "product_id": "42806-413_4bde68a6-0945-b21f-e063-6394a90a3bc4", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "42806-413", "generic_name": "bupropion hydrochloride", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "brand_name_suffix": "SR", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA216766", "marketing_category": "ANDA", "marketing_start_date": "20230228", "listing_expiration_date": "20271231"}