Package 70518-2929-0

Brand: trazodone hydrochloride

Generic: trazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2929-0
Digits Only 7051829290
Product NDC 70518-2929
Product ID 70518-2929_4ab481a2-6844-7d94-e063-6394a90a751d
Description

30 TABLET in 1 BLISTER PACK (70518-2929-0)

Marketing

Marketing Status
Marketed Since 2020-10-31
Brand trazodone hydrochloride
Generic trazodone hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4ab481a2-6844-7d94-e063-6394a90a751d", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856377"], "spl_set_id": ["38e9820a-6edc-4bf5-b5e4-034b9e48b583"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2929-0)", "package_ndc": "70518-2929-0", "marketing_start_date": "20201031"}], "brand_name": "Trazodone Hydrochloride", "product_id": "70518-2929_4ab481a2-6844-7d94-e063-6394a90a751d", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "70518-2929", "generic_name": "Trazodone Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA071523", "marketing_category": "ANDA", "marketing_start_date": "20201031", "listing_expiration_date": "20271231"}