Package 0904-6868-61

Brand: trazodone hydrochloride

Generic: trazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-6868-61
Digits Only 0904686861
Product NDC 0904-6868
Description

100 BLISTER PACK in 1 CARTON (0904-6868-61) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2017-12-11
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": "1bfc986d-82a1-4503-8eea-7ebf3186d09d", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856364", "856373", "856377"], "spl_set_id": ["8eb85c26-a6cb-4a10-a990-ccc0b20aff08"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6868-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6868-61", "marketing_start_date": "20171211"}], "brand_name": "Trazodone Hydrochloride", "product_id": "0904-6868_1bfc986d-82a1-4503-8eea-7ebf3186d09d", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "0904-6868", "generic_name": "Trazodone Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA205253", "marketing_category": "ANDA", "marketing_start_date": "20171211", "listing_expiration_date": "20261231"}