Package 42806-349-09

Brand: bupropion hydrochloride xl

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42806-349-09
Digits Only 4280634909
Product NDC 42806-349
Product ID 42806-349_b271a757-875d-4349-8c40-a047c10cbd1b
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-349-09)

Marketing

Marketing Status
Marketed Since 2017-10-01
Brand bupropion hydrochloride xl
Generic bupropion hydrochloride
Sample Package No

Linked Drug Pages (1)

Bupropion Hydrochloride XL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b271a757-875d-4349-8c40-a047c10cbd1b", "openfda": {"upc": ["0342806349090"], "unii": ["ZG7E5POY8O"], "rxcui": ["993541", "993557"], "spl_set_id": ["178c7129-a752-4ad9-ac82-4473e23bbacc"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-349-05)", "package_ndc": "42806-349-05", "marketing_start_date": "20171001"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-349-09)", "package_ndc": "42806-349-09", "marketing_start_date": "20171001"}], "brand_name": "Bupropion Hydrochloride XL", "product_id": "42806-349_b271a757-875d-4349-8c40-a047c10cbd1b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "42806-349", "generic_name": "Bupropion Hydrochloride", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "brand_name_suffix": "XL", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA207224", "marketing_category": "ANDA", "marketing_start_date": "20171001", "listing_expiration_date": "20261231"}