Package 70518-2106-0

Brand: trifluoperazine hydrochloride

Generic: trifluoperazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2106-0
Digits Only 7051821060
Product NDC 70518-2106
Product ID 70518-2106_499eec4f-0c75-67a3-e063-6394a90aa9de
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2106-0)

Marketing

Marketing Status
Marketed Since 2019-05-23
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": "499eec4f-0c75-67a3-e063-6394a90aa9de", "openfda": {"unii": ["6P1Y2SNF5V"], "rxcui": ["198325"], "spl_set_id": ["6a05900b-ca43-483a-a460-8ac378653f12"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2106-0)", "package_ndc": "70518-2106-0", "marketing_start_date": "20190523"}], "brand_name": "Trifluoperazine Hydrochloride", "product_id": "70518-2106_499eec4f-0c75-67a3-e063-6394a90aa9de", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-2106", "generic_name": "trifluoperazine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trifluoperazine Hydrochloride", "active_ingredients": [{"name": "TRIFLUOPERAZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA040209", "marketing_category": "ANDA", "marketing_start_date": "20190523", "listing_expiration_date": "20271231"}