Package 68071-2256-1

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-2256-1
Digits Only 6807122561
Product NDC 68071-2256
Product ID 68071-2256_1d7692c3-44e2-f52d-e063-6394a90aa73f
Description

100 TABLET, FILM COATED in 1 BOTTLE (68071-2256-1)

Marketing

Marketing Status
Marketed Since 2020-09-10
Brand bupropion hydrochloride
Generic bupropion hydrochloride
Sample Package No

Linked Drug Pages (1)

Bupropion Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1d7692c3-44e2-f52d-e063-6394a90aa73f", "openfda": {"upc": ["0368071225617"], "unii": ["ZG7E5POY8O"], "rxcui": ["993691"], "spl_set_id": ["aef84c3a-68e2-e9d9-e053-2995a90a4ab8"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68071-2256-1)", "package_ndc": "68071-2256-1", "marketing_start_date": "20200910"}], "brand_name": "Bupropion Hydrochloride", "product_id": "68071-2256_1d7692c3-44e2-f52d-e063-6394a90aa73f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "68071-2256", "generic_name": "Bupropion Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA076143", "marketing_category": "ANDA", "marketing_start_date": "20060117", "listing_expiration_date": "20261231"}