Package 62332-118-91

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62332-118-91
Digits Only 6233211891
Product NDC 62332-118
Product ID 62332-118_ee494cd8-6374-4c6a-86f6-722c999e43e1
Description

1000 TABLET, FILM COATED in 1 BOTTLE (62332-118-91)

Marketing

Marketing Status
Marketed Since 2024-01-10
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": "ee494cd8-6374-4c6a-86f6-722c999e43e1", "openfda": {"upc": ["0362332118311", "0362332127313"], "unii": ["ZG7E5POY8O"], "rxcui": ["993687", "993691"], "spl_set_id": ["b303a0ad-5971-44ab-937c-bcf3ff650358"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62332-118-31)", "package_ndc": "62332-118-31", "marketing_start_date": "20240110"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62332-118-91)", "package_ndc": "62332-118-91", "marketing_start_date": "20240110"}], "brand_name": "Bupropion Hydrochloride", "product_id": "62332-118_ee494cd8-6374-4c6a-86f6-722c999e43e1", "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": "62332-118", "generic_name": "Bupropion Hydrochloride", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA203013", "marketing_category": "ANDA", "marketing_start_date": "20240110", "listing_expiration_date": "20261231"}