Package 70518-2095-0

Brand: trifluoperazine hydrochloride

Generic: trifluoperazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2095-0
Digits Only 7051820950
Product NDC 70518-2095
Product ID 70518-2095_499dd16d-513b-780e-e063-6294a90a0230
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2095-0)

Marketing

Marketing Status
Marketed Since 2019-05-21
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": "499dd16d-513b-780e-e063-6294a90a0230", "openfda": {"unii": ["6P1Y2SNF5V"], "rxcui": ["198324"], "spl_set_id": ["339ceb53-3b1c-459f-84eb-77bd4315c998"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2095-0)", "package_ndc": "70518-2095-0", "marketing_start_date": "20190521"}], "brand_name": "Trifluoperazine Hydrochloride", "product_id": "70518-2095_499dd16d-513b-780e-e063-6294a90a0230", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-2095", "generic_name": "trifluoperazine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trifluoperazine Hydrochloride", "active_ingredients": [{"name": "TRIFLUOPERAZINE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA040209", "marketing_category": "ANDA", "marketing_start_date": "20190521", "listing_expiration_date": "20271231"}