Package 71335-2649-2

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2649-2
Digits Only 7133526492
Product NDC 71335-2649
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-2)

Marketing

Marketing Status
Marketed Since 2025-06-03
Brand bupropion hydrochloride
Generic bupropion hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "82d4ffc2-489f-4fee-acdf-ab5c72910464", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993503"], "spl_set_id": ["c5d55b0c-8b81-476a-994e-1989e2a56255"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-1)", "package_ndc": "71335-2649-1", "marketing_start_date": "20250603"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-2)", "package_ndc": "71335-2649-2", "marketing_start_date": "20250603"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-3)", "package_ndc": "71335-2649-3", "marketing_start_date": "20250603"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-4)", "package_ndc": "71335-2649-4", "marketing_start_date": "20250603"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-5)", "package_ndc": "71335-2649-5", "marketing_start_date": "20250603"}, {"sample": false, "description": "15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-6)", "package_ndc": "71335-2649-6", "marketing_start_date": "20250603"}, {"sample": false, "description": "21 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-7)", "package_ndc": "71335-2649-7", "marketing_start_date": "20250603"}], "brand_name": "Bupropion hydrochloride", "product_id": "71335-2649_82d4ffc2-489f-4fee-acdf-ab5c72910464", "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": "71335-2649", "generic_name": "Bupropion hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA216800", "marketing_category": "ANDA", "marketing_start_date": "20230531", "listing_expiration_date": "20261231"}