Package 24979-247-06

Brand: forfivo xl

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 24979-247-06
Digits Only 2497924706
Product NDC 24979-247
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-247-06)

Marketing

Marketing Status
Marketed Since 2023-12-15
Brand forfivo 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": "96a5dcb3-5d09-4357-96e3-8005ef094b2c", "openfda": {"upc": ["0324979247069"], "unii": ["ZG7E5POY8O"], "rxcui": ["1232585", "1232591"], "spl_set_id": ["80b01182-dc94-4990-8ebb-55c306d7e536"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-247-06)", "package_ndc": "24979-247-06", "marketing_start_date": "20231215"}], "brand_name": "Forfivo XL", "product_id": "24979-247_96a5dcb3-5d09-4357-96e3-8005ef094b2c", "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": "24979-247", "generic_name": "bupropion hydrochloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Forfivo", "brand_name_suffix": "XL", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "450 mg/1"}], "application_number": "NDA022497", "marketing_category": "NDA", "marketing_start_date": "20231215", "listing_expiration_date": "20261231"}