Package 70518-2180-2

Brand: trazodone hydrochloride

Generic: trazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2180-2
Digits Only 7051821802
Product NDC 70518-2180
Description

30 TABLET in 1 BOTTLE, PLASTIC (70518-2180-2)

Marketing

Marketing Status
Marketed Since 2025-10-17
Brand trazodone hydrochloride
Generic trazodone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "49db46f7-1ae9-7c94-e063-6294a90a94e3", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856364"], "spl_set_id": ["2863317d-657b-4dc6-81fb-b7158ea03498"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-2180-2)", "package_ndc": "70518-2180-2", "marketing_start_date": "20251017"}], "brand_name": "Trazodone Hydrochloride", "product_id": "70518-2180_49db46f7-1ae9-7c94-e063-6294a90a94e3", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "70518-2180", "generic_name": "Trazodone Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA205253", "marketing_category": "ANDA", "marketing_start_date": "20190701", "listing_expiration_date": "20271231"}