Package 60687-340-01

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-340-01
Digits Only 6068734001
Product NDC 60687-340
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-340-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-340-11)

Marketing

Marketing Status
Marketed Since 2018-02-01
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": "235ba423-7e33-5634-e063-6394a90a49da", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993687", "993691"], "spl_set_id": ["88c980c8-aaa8-4378-9ac2-24d588640caa"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-340-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-340-11)", "package_ndc": "60687-340-01", "marketing_start_date": "20180201"}], "brand_name": "Bupropion Hydrochloride", "product_id": "60687-340_235ba423-7e33-5634-e063-6394a90a49da", "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": "60687-340", "generic_name": "Bupropion Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA076143", "marketing_category": "ANDA", "marketing_start_date": "20180201", "listing_expiration_date": "20261231"}