Package 70518-3426-1

Brand: trazodone hydrochloride

Generic: trazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3426-1
Digits Only 7051834261
Product NDC 70518-3426
Description

90 TABLET in 1 BOTTLE, PLASTIC (70518-3426-1)

Marketing

Marketing Status
Marketed Since 2024-05-29
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": "415bb0e0-6a4b-89b7-e063-6294a90aed12", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856373"], "spl_set_id": ["acd077db-e2b8-4d29-94c0-128439050c66"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-3426-1)", "package_ndc": "70518-3426-1", "marketing_start_date": "20240529"}], "brand_name": "Trazodone Hydrochloride", "product_id": "70518-3426_415bb0e0-6a4b-89b7-e063-6294a90aed12", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "70518-3426", "generic_name": "Trazodone Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA202180", "marketing_category": "ANDA", "marketing_start_date": "20220525", "listing_expiration_date": "20261231"}