Package 70518-3479-1

Brand: trazodone hydrochloride

Generic: trazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3479-1
Digits Only 7051834791
Product NDC 70518-3479
Product ID 70518-3479_43cf5367-627b-9082-e063-6394a90a1aeb
Description

30 TABLET in 1 BLISTER PACK (70518-3479-1)

Marketing

Marketing Status
Marketed Since 2023-05-24
Brand trazodone hydrochloride
Generic trazodone hydrochloride
Sample Package No

Linked Drug Pages (1)

Trazodone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "43cf5367-627b-9082-e063-6394a90a1aeb", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856364"], "spl_set_id": ["1f74b23d-f2eb-4c18-a583-d608b7713694"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3479-1)", "package_ndc": "70518-3479-1", "marketing_start_date": "20230524"}], "brand_name": "Trazodone Hydrochloride", "product_id": "70518-3479_43cf5367-627b-9082-e063-6394a90a1aeb", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "70518-3479", "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": "ANDA202180", "marketing_category": "ANDA", "marketing_start_date": "20220816", "listing_expiration_date": "20261231"}