Package 57664-014-72

Brand: trazodone hydrochloride

Generic: trazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 57664-014-72
Digits Only 5766401472
Product NDC 57664-014
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-014-72)

Marketing

Marketing Status
Marketed Since 2022-10-03
Brand trazodone hydrochloride
Generic trazodone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "323e3d63-4d8d-7088-e063-6294a90abb0f", "openfda": {"upc": ["0357664014721"], "unii": ["6E8ZO8LRNM"], "rxcui": ["856364", "856373", "856377"], "spl_set_id": ["f291b905-a739-5e43-e053-2995a90ac40c"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-014-72)", "package_ndc": "57664-014-72", "marketing_start_date": "20221003"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-014-74)", "package_ndc": "57664-014-74", "marketing_start_date": "20221003"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-014-75)", "package_ndc": "57664-014-75", "marketing_start_date": "20221003"}], "brand_name": "Trazodone Hydrochloride", "product_id": "57664-014_323e3d63-4d8d-7088-e063-6294a90abb0f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "57664-014", "generic_name": "Trazodone Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, 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": "20221003", "listing_expiration_date": "20261231"}