Package 72789-079-30

Brand: trazodone hydrochloride

Generic: trazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-079-30
Digits Only 7278907930
Product NDC 72789-079
Product ID 72789-079_4019c854-3393-5b53-e063-6394a90abd16
Description

30 TABLET in 1 BOTTLE, PLASTIC (72789-079-30)

Marketing

Marketing Status
Marketed Since 2020-04-06
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": "4019c854-3393-5b53-e063-6394a90abd16", "openfda": {"upc": ["0372789079301"], "unii": ["6E8ZO8LRNM"], "rxcui": ["856364"], "spl_set_id": ["9b022ae9-dd52-43ae-804b-ddf8e7cfd530"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-079-30)", "package_ndc": "72789-079-30", "marketing_start_date": "20200406"}], "brand_name": "Trazodone Hydrochloride", "product_id": "72789-079_4019c854-3393-5b53-e063-6394a90abd16", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "72789-079", "generic_name": "Trazodone Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA071525", "marketing_category": "ANDA", "marketing_start_date": "20200311", "listing_expiration_date": "20261231"}