Package 60760-781-30

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-781-30
Digits Only 6076078130
Product NDC 60760-781
Product ID 60760-781_36250235-1dde-a8c7-e063-6294a90a7fc3
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-781-30)

Marketing

Marketing Status
Marketed Since 2025-05-21
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": "36250235-1dde-a8c7-e063-6294a90a7fc3", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993687"], "spl_set_id": ["362504fd-2f0a-c097-e063-6394a90ac0fc"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-781-30)", "package_ndc": "60760-781-30", "marketing_start_date": "20250521"}], "brand_name": "Bupropion Hydrochloride", "product_id": "60760-781_36250235-1dde-a8c7-e063-6294a90a7fc3", "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": "60760-781", "generic_name": "Bupropion Hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "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"}