Package 70518-3756-0

Brand: trazodone hydrochloride

Generic: trazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3756-0
Digits Only 7051837560
Product NDC 70518-3756
Description

30 TABLET in 1 BLISTER PACK (70518-3756-0)

Marketing

Marketing Status
Marketed Since 2023-06-11
Brand trazodone hydrochloride
Generic trazodone hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c580281-e6e4-e007-e063-6294a90a36cf", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856373"], "spl_set_id": ["fec78f5d-2567-44d3-9f04-1a6913357019"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3756-0)", "package_ndc": "70518-3756-0", "marketing_start_date": "20230611"}], "brand_name": "TRAZODONE HYDROCHLORIDE", "product_id": "70518-3756_3c580281-e6e4-e007-e063-6294a90a36cf", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "70518-3756", "generic_name": "TRAZODONE HYDROCHLORIDE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAZODONE HYDROCHLORIDE", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA204852", "marketing_category": "ANDA", "marketing_start_date": "20230611", "listing_expiration_date": "20261231"}