Package 0904-7530-60

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7530-60
Digits Only 0904753060
Product NDC 0904-7530
Description

100 TABLET in 1 BOTTLE (0904-7530-60)

Marketing

Marketing Status
Marketed Since 2025-01-30
Brand bupropion hydrochloride
Generic bupropion hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "413f7114-b680-46d3-bd56-e92420268b6d", "openfda": {"upc": ["0309047530601", "0309047529605"], "unii": ["ZG7E5POY8O"], "rxcui": ["993687", "993691"], "spl_set_id": ["3c6b5ab4-9671-4fcd-8b4c-7f230dcfe6c9"], "manufacturer_name": ["MAJOR PHARMACEUTICALS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0904-7530-60)", "package_ndc": "0904-7530-60", "marketing_start_date": "20250130"}], "brand_name": "Bupropion Hydrochloride", "product_id": "0904-7530_413f7114-b680-46d3-bd56-e92420268b6d", "dosage_form": "TABLET", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "0904-7530", "generic_name": "Bupropion Hydrochloride", "labeler_name": "MAJOR PHARMACEUTICALS", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA206975", "marketing_category": "ANDA", "marketing_start_date": "20250130", "listing_expiration_date": "20261231"}