Package 71335-2378-2
Brand: bupropion hydrochloride xl
Generic: bupropion hydrochloridePackage Facts
Identity
Package NDC
71335-2378-2
Digits Only
7133523782
Product NDC
71335-2378
Description
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2378-2)
Marketing
Marketing Status
Brand
bupropion hydrochloride xl
Generic
bupropion hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d9807f26-dfac-45a6-8279-83c1f54a113e", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993541"], "spl_set_id": ["eb25adb1-9841-42ce-aa22-718fb0fba5dd"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2378-1)", "package_ndc": "71335-2378-1", "marketing_start_date": "20240416"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2378-2)", "package_ndc": "71335-2378-2", "marketing_start_date": "20240612"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2378-3)", "package_ndc": "71335-2378-3", "marketing_start_date": "20240327"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2378-4)", "package_ndc": "71335-2378-4", "marketing_start_date": "20250131"}, {"sample": false, "description": "14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2378-5)", "package_ndc": "71335-2378-5", "marketing_start_date": "20250131"}], "brand_name": "Bupropion Hydrochloride XL", "product_id": "71335-2378_d9807f26-dfac-45a6-8279-83c1f54a113e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "71335-2378", "generic_name": "bupropion hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "brand_name_suffix": "XL", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA210015", "marketing_category": "ANDA", "marketing_start_date": "20230430", "listing_expiration_date": "20261231"}