Package 63187-952-60
Brand: bupropion hydrochloride sr
Generic: bupropion hydrochloridePackage Facts
Identity
Package NDC
63187-952-60
Digits Only
6318795260
Product NDC
63187-952
Description
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-952-60)
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": "3bfee467-f720-4aa7-aeff-6b07c1618808", "openfda": {"upc": ["0363187952600"], "unii": ["ZG7E5POY8O"], "rxcui": ["993503"], "spl_set_id": ["b59d950c-341f-45f1-b5b2-d64ccc799580"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-952-14)", "package_ndc": "63187-952-14", "marketing_start_date": "20240507"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-952-30)", "package_ndc": "63187-952-30", "marketing_start_date": "20180101"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-952-60)", "package_ndc": "63187-952-60", "marketing_start_date": "20180101"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-952-90)", "package_ndc": "63187-952-90", "marketing_start_date": "20180101"}], "brand_name": "Bupropion Hydrochloride SR", "product_id": "63187-952_3bfee467-f720-4aa7-aeff-6b07c1618808", "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": "63187-952", "generic_name": "bupropion hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "brand_name_suffix": "SR", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA079095", "marketing_category": "ANDA", "marketing_start_date": "20090324", "listing_expiration_date": "20261231"}