Package 70518-3787-1

Brand: bupropion hydrochloride sr

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3787-1
Digits Only 7051837871
Product NDC 70518-3787
Product ID 70518-3787_3c571320-469c-2a26-e063-6294a90a0877
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3787-1)

Marketing

Marketing Status
Marketed Since 2025-08-14
Brand bupropion hydrochloride sr
Generic bupropion hydrochloride
Sample Package No

Linked Drug Pages (1)

Bupropion Hydrochloride SR ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3c571320-469c-2a26-e063-6294a90a0877", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993503"], "spl_set_id": ["c76f2f9f-3999-4bdd-8ec3-e0066318d378"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3787-1)", "package_ndc": "70518-3787-1", "marketing_start_date": "20250814"}], "brand_name": "Bupropion Hydrochloride SR", "product_id": "70518-3787_3c571320-469c-2a26-e063-6294a90a0877", "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": "70518-3787", "generic_name": "bupropion hydrochloride", "labeler_name": "REMEDYREPACK INC.", "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": "ANDA205794", "marketing_category": "ANDA", "marketing_start_date": "20230712", "listing_expiration_date": "20261231"}