Package 70518-4363-1

Brand: trazodone hydrochloride

Generic: trazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4363-1
Digits Only 7051843631
Product NDC 70518-4363
Product ID 70518-4363_39a96071-618e-9b79-e063-6394a90a03ef
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4363-1)

Marketing

Marketing Status
Marketed Since 2025-07-11
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": "39a96071-618e-9b79-e063-6394a90a03ef", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856377"], "spl_set_id": ["fa7afa93-b98c-4dc7-bbb8-ab6a058427b9"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4363-0)", "package_ndc": "70518-4363-0", "marketing_start_date": "20250618"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4363-1)", "package_ndc": "70518-4363-1", "marketing_start_date": "20250711"}], "brand_name": "Trazodone Hydrochloride", "product_id": "70518-4363_39a96071-618e-9b79-e063-6394a90a03ef", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "70518-4363", "generic_name": "Trazodone Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA073137", "marketing_category": "ANDA", "marketing_start_date": "20250618", "listing_expiration_date": "20261231"}