Package 70518-3707-0

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3707-0
Digits Only 7051837070
Product NDC 70518-3707
Product ID 70518-3707_3b122509-7283-b29e-e063-6294a90a3903
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3707-0)

Marketing

Marketing Status
Marketed Since 2023-04-10
Brand fluphenazine hydrochloride
Generic fluphenazine hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3b122509-7283-b29e-e063-6294a90a3903", "openfda": {"unii": ["ZOU145W1XL"], "rxcui": ["860918"], "spl_set_id": ["f68bacd4-3205-4735-996f-9e953e83cf48"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3707-0)", "package_ndc": "70518-3707-0", "marketing_start_date": "20230410"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "70518-3707_3b122509-7283-b29e-e063-6294a90a3903", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-3707", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA215848", "marketing_category": "ANDA", "marketing_start_date": "20230410", "listing_expiration_date": "20261231"}