Package 71335-3025-1

Brand: trazodone hydrochloride

Generic: trazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-3025-1
Digits Only 7133530251
Product NDC 71335-3025
Product ID 71335-3025_32cd8f4d-4db4-477b-b8af-0517499dc856
Description

500 TABLET in 1 BOTTLE (71335-3025-1)

Marketing

Marketing Status
Marketed Since 2025-12-04
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": "32cd8f4d-4db4-477b-b8af-0517499dc856", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856369"], "spl_set_id": ["470a98a2-4e68-4c98-b3c8-e5eba4e55cdc"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (71335-3025-1)", "package_ndc": "71335-3025-1", "marketing_start_date": "20251204"}], "brand_name": "TRAZODONE HYDROCHLORIDE", "product_id": "71335-3025_32cd8f4d-4db4-477b-b8af-0517499dc856", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "71335-3025", "generic_name": "TRAZODONE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAZODONE HYDROCHLORIDE", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA204852", "marketing_category": "ANDA", "marketing_start_date": "20150915", "listing_expiration_date": "20261231"}