Package 72189-457-30

Brand: bupropion hcl

Generic: bupropion hcl
NDC Package

Package Facts

Identity

Package NDC 72189-457-30
Digits Only 7218945730
Product NDC 72189-457
Product ID 72189-457_2c4dd247-ae5a-fe93-e063-6394a90a937c
Description

30 TABLET, FILM COATED in 1 BOTTLE (72189-457-30)

Marketing

Marketing Status
Marketed Since 2023-03-30
Brand bupropion hcl
Generic bupropion hcl
Sample Package No

Linked Drug Pages (1)

Bupropion HCL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4dd247-ae5a-fe93-e063-6394a90a937c", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993687"], "spl_set_id": ["f820ad7d-3c88-4a4f-e053-6294a90aef7b"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-457-30)", "package_ndc": "72189-457-30", "marketing_start_date": "20230330"}], "brand_name": "Bupropion HCL", "product_id": "72189-457_2c4dd247-ae5a-fe93-e063-6394a90a937c", "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": "72189-457", "generic_name": "Bupropion HCL", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion HCL", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA076143", "marketing_category": "ANDA", "marketing_start_date": "20230330", "listing_expiration_date": "20261231"}