Package 70518-4554-0

Brand: trifluoperazine hydrochloride

Generic: trifluoperazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4554-0
Digits Only 7051845540
Product NDC 70518-4554
Product ID 70518-4554_49100707-9fb9-e678-e063-6394a90a8146
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4554-0)

Marketing

Marketing Status
Marketed Since 2026-01-23
Brand trifluoperazine hydrochloride
Generic trifluoperazine hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49100707-9fb9-e678-e063-6394a90a8146", "openfda": {"unii": ["6P1Y2SNF5V"], "rxcui": ["198324"], "spl_set_id": ["069d3469-138b-4e4f-a7bb-6acac5f86abb"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4554-0)", "package_ndc": "70518-4554-0", "marketing_start_date": "20260123"}], "brand_name": "Trifluoperazine Hydrochloride", "product_id": "70518-4554_49100707-9fb9-e678-e063-6394a90a8146", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-4554", "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": "ANDA085786", "marketing_category": "ANDA", "marketing_start_date": "20260123", "listing_expiration_date": "20271231"}