Package 0781-8034-01

Brand: trifluoperazine hydrochloride

Generic: trifluoperazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0781-8034-01
Digits Only 0781803401
Product NDC 0781-8034
Product ID 0781-8034_79bbd43c-c3f3-4fa5-a2a4-88868251febb
Description

100 TABLET, FILM COATED in 1 BOTTLE (0781-8034-01)

Marketing

Marketing Status
Marketed Since 2019-01-14
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": "79bbd43c-c3f3-4fa5-a2a4-88868251febb", "openfda": {"unii": ["6P1Y2SNF5V"], "rxcui": ["198322", "198323", "198324", "198325"], "spl_set_id": ["ae43c10e-cfa9-4298-8af5-7a3e6524bbda"], "manufacturer_name": ["Sandoz Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0781-8034-01)", "package_ndc": "0781-8034-01", "marketing_start_date": "20190114"}], "brand_name": "Trifluoperazine Hydrochloride", "product_id": "0781-8034_79bbd43c-c3f3-4fa5-a2a4-88868251febb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0781-8034", "generic_name": "Trifluoperazine Hydrochloride", "labeler_name": "Sandoz Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trifluoperazine Hydrochloride", "active_ingredients": [{"name": "TRIFLUOPERAZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA085789", "marketing_category": "ANDA", "marketing_start_date": "19811120", "listing_expiration_date": "20261231"}