Package 72162-2204-1

Brand: trifluoperazine hydrochloride

Generic: trifluoperazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2204-1
Digits Only 7216222041
Product NDC 72162-2204
Product ID 72162-2204_19b76401-6790-44f7-b756-b078948bbf12
Description

100 TABLET, FILM COATED in 1 BOTTLE (72162-2204-1)

Marketing

Marketing Status
Discontinued 2027-03-19
Brand trifluoperazine hydrochloride
Generic trifluoperazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Trifluoperazine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "19b76401-6790-44f7-b756-b078948bbf12", "openfda": {"unii": ["6P1Y2SNF5V"], "rxcui": ["198322"], "spl_set_id": ["19b76401-6790-44f7-b756-b078948bbf12"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-2204-1)", "package_ndc": "72162-2204-1", "marketing_end_date": "20270319", "marketing_start_date": "20240402"}], "brand_name": "Trifluoperazine Hydrochloride", "product_id": "72162-2204_19b76401-6790-44f7-b756-b078948bbf12", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "72162-2204", "generic_name": "Trifluoperazine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trifluoperazine Hydrochloride", "active_ingredients": [{"name": "TRIFLUOPERAZINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA085785", "marketing_category": "ANDA", "marketing_end_date": "20270319", "marketing_start_date": "19811120"}