Package 62135-724-90
Brand: bupropion hydrochloride
Generic: bupropion hydrochloridePackage Facts
Identity
Package NDC
62135-724-90
Digits Only
6213572490
Product NDC
62135-724
Description
90 TABLET in 1 BOTTLE (62135-724-90)
Marketing
Marketing Status
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": "2470b0cc-d408-d52f-e063-6394a90ab698", "openfda": {"upc": ["0362135724900", "0362135723903"], "unii": ["ZG7E5POY8O"], "rxcui": ["993687", "993691"], "spl_set_id": ["620fab1e-aafb-444d-ab81-63281cd139c5"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-724-90)", "package_ndc": "62135-724-90", "marketing_start_date": "20230811"}], "brand_name": "Bupropion Hydrochloride", "product_id": "62135-724_2470b0cc-d408-d52f-e063-6394a90ab698", "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": "62135-724", "generic_name": "Bupropion Hydrochloride", "labeler_name": "Chartwell RX, LLC", "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": "20160819", "listing_expiration_date": "20261231"}