Package 0555-0711-02

Brand: trazodone hydrochloride

Generic: trazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0555-0711-02
Digits Only 0555071102
Product NDC 0555-0711
Product ID 0555-0711_3902eb87-aa22-4775-b56a-7cb86c5f920e
Description

100 TABLET in 1 BOTTLE (0555-0711-02)

Marketing

Marketing Status
Marketed Since 2021-12-09
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": "3902eb87-aa22-4775-b56a-7cb86c5f920e", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856369"], "spl_set_id": ["9c4da6ad-d4d1-4e8c-918d-8ac48512a93f"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0555-0711-02)", "package_ndc": "0555-0711-02", "marketing_start_date": "20211209"}], "brand_name": "Trazodone Hydrochloride", "product_id": "0555-0711_3902eb87-aa22-4775-b56a-7cb86c5f920e", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "0555-0711", "generic_name": "Trazodone Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA071196", "marketing_category": "ANDA", "marketing_start_date": "20211209", "listing_expiration_date": "20261231"}