Package 68001-309-00

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68001-309-00
Digits Only 6800130900
Product NDC 68001-309
Product ID 68001-309_44a42976-faae-065e-e063-6394a90aa7da
Description

100 TABLET, FILM COATED in 1 BOTTLE (68001-309-00)

Marketing

Marketing Status
Marketed Since 2017-02-08
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": "44a42976-faae-065e-e063-6394a90aa7da", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993687", "993691"], "spl_set_id": ["7d035056-44ab-444d-9d27-125b3f571140"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68001-309-00)", "package_ndc": "68001-309-00", "marketing_start_date": "20170208"}], "brand_name": "Bupropion Hydrochloride", "product_id": "68001-309_44a42976-faae-065e-e063-6394a90aa7da", "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": "68001-309", "generic_name": "Bupropion Hydrochloride", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA076143", "marketing_category": "ANDA", "marketing_start_date": "20060117", "listing_expiration_date": "20261231"}