Package 24689-120-01

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 24689-120-01
Digits Only 2468912001
Product NDC 24689-120
Description

100 TABLET, FILM COATED in 1 BOTTLE (24689-120-01)

Marketing

Marketing Status
Marketed Since 2021-12-20
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": "120b51f0-f2d3-1de1-e063-6294a90a3691", "openfda": {"upc": ["0324689119014", "0324689120010"], "unii": ["ZG7E5POY8O"], "rxcui": ["993687", "993691"], "spl_set_id": ["d1830cfd-e7f4-345c-e053-2995a90a2251"], "manufacturer_name": ["Apnar Pharma LP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (24689-120-01)", "package_ndc": "24689-120-01", "marketing_start_date": "20211220"}], "brand_name": "Bupropion Hydrochloride", "product_id": "24689-120_120b51f0-f2d3-1de1-e063-6294a90a3691", "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": "24689-120", "generic_name": "Bupropion Hydrochloride", "labeler_name": "Apnar Pharma LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA075584", "marketing_category": "ANDA", "marketing_start_date": "20211220", "listing_expiration_date": "20261231"}