Package 68788-7807-2
Brand: bupropion hydrochloride sr
Generic: bupropion hydrochloridePackage Facts
Identity
Package NDC
68788-7807-2
Digits Only
6878878072
Product NDC
68788-7807
Description
20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-2)
Marketing
Marketing Status
Brand
bupropion hydrochloride sr
Generic
bupropion hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "62bfa69e-b220-40eb-9c76-334adefbaa01", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993518"], "spl_set_id": ["0b33fb1f-a7f0-4ab7-a882-eca2d2c77afa"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-1)", "package_ndc": "68788-7807-1", "marketing_start_date": "20201028"}, {"sample": false, "description": "20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-2)", "package_ndc": "68788-7807-2", "marketing_start_date": "20201028"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-3)", "package_ndc": "68788-7807-3", "marketing_start_date": "20201028"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-6)", "package_ndc": "68788-7807-6", "marketing_start_date": "20201028"}, {"sample": false, "description": "120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-8)", "package_ndc": "68788-7807-8", "marketing_start_date": "20201028"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-9)", "package_ndc": "68788-7807-9", "marketing_start_date": "20201028"}], "brand_name": "Bupropion Hydrochloride SR", "product_id": "68788-7807_62bfa69e-b220-40eb-9c76-334adefbaa01", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "68788-7807", "generic_name": "bupropion hydrochloride", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "brand_name_suffix": "SR", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA205794", "marketing_category": "ANDA", "marketing_start_date": "20201028", "listing_expiration_date": "20261231"}