Package 72162-2400-1

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2400-1
Digits Only 7216224001
Product NDC 72162-2400
Product ID 72162-2400_b8a80536-7312-4576-8cd2-7f8002e180b5
Description

100 TABLET in 1 BOTTLE (72162-2400-1)

Marketing

Marketing Status
Marketed Since 2024-10-02
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": "b8a80536-7312-4576-8cd2-7f8002e180b5", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993691"], "spl_set_id": ["bd99969d-03d5-4609-88e8-a9ae93a83907"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2400-1)", "package_ndc": "72162-2400-1", "marketing_start_date": "20241002"}], "brand_name": "bupropion Hydrochloride", "product_id": "72162-2400_b8a80536-7312-4576-8cd2-7f8002e180b5", "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": "72162-2400", "generic_name": "bupropion Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA206975", "marketing_category": "ANDA", "marketing_start_date": "20160819", "listing_expiration_date": "20261231"}